R. Gorlin

G. Clayman, R. Gorlin, G. Adams, 1992, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

The syndrome of pits of the lower lip and cleft lip and/or palate. Genetic considerations.

V. Anderson, R. Gorlin, J. Červenka, 1967, American journal of human genetics.

Syndromes of facial clefting.

R. Gorlin, J. Červenka, 1974, Scandinavian journal of plastic and reconstructive surgery.

Genetic disorders affecting mucous membranes.

R. Gorlin, Robert J. Gorlin, 1969, Oral surgery, oral medicine, and oral pathology.

Unusual stomadromes--pachyonchia congenita, lipoid proteinosis, Reiter's syndrome, epidermolysis bullosa, Bonnevie-Ullrich-Turner's syndrome, and multiple hereditary telangiectasia.

R. Gorlin, A. Chaudhry, 1960, Oral surgery, oral medicine, and oral pathology.

Oral lesions accompanying pachyonychia congenita.

R. Gorlin, A. Chaudhry, 1958, Oral surgery, oral medicine, and oral pathology.

Leukonychia totalis, multiple sebaceous cysts, and renal calculi. A syndrome.

R. Gorlin, L. L. Bushkell, 1975, Archives of dermatology.

Assessment of hypoxia in the human heart.

R. Gorlin, 1972, Cardiology.

International classification of osteochondrodysplasias

D. Sillence, A. Poznanski, P. Beighton, 1992, European Journal of Pediatrics.

International nomenclature and classification of the osteochondrodysplasias (1997) international working group on constitutional diseases of bone

D. Sillence, S. Mundlos, I. Kaitila, 1998 .

Cranio-carop-tarsal dysplasia or the whistling face syndrome. I. Clinical considerations.

R. Gorlin, S. Weinstein, 1969, American journal of diseases of children.

Focal dermal hypoplasia syndrome.

R. Gorlin, H. Sedano, L. Ginsburg, 1970, The American journal of roentgenology, radium therapy, and nuclear medicine.

Focal dermal hypoplasia

W. C. Peterson, R. Gorlin, R. Goltz, 2019, Definitions.

Multiple schwannomas, multiple nevi, and multiple vaginal leiomyomas: a new dominant syndrome.

R. Gorlin, I. Koutlas, 1998, American journal of medical genetics.

Noonan-like/multiple giant cell lesion syndrome.

R. Gorlin, M. Cohen, M. Michael Cohen, 1991, American journal of medical genetics.

Pycnodysostosis. Clinical and genetic considerations.

V. Anderson, R. Gorlin, H. Sedano, 1968, American journal of diseases of children.

WHIM syndrome, an autosomal dominant disorder: clinical, hematological, and molecular studies.

B. Gelb, M. Pittelkow, R. Gorlin, 2000, American journal of medical genetics.

Odontogenic tumors in mammals and fish.

R. Gorlin, 1972, Oral surgery, oral medicine, and oral pathology.

The oral pathology of domesticated animals.

R. Gorlin, A. Chaudhry, J. J. Clark, 1958, Oral surgery, oral medicine, and oral pathology.

Gorlin's Syndromes of the Head and Neck

I. Krantz, R. Hennekam, J. Allanson, 2010 .

Germline mutations in PTEN are present in Bannayan-Zonana syndrome

C. Eng, R. Parsons, D. Liaw, 1997, Nature Genetics.

patients with Cowden d isease

M. Nelen, H. Kremer, J. Fryns, 1997 .

Multiple hamartoma syndrome (Cowden's disease).

P. Weary, R. Gorlin, K. Greer, 1972, Archives of dermatology.

Systemic Inherited Disorders with Involvement of Multiple Oral Structures

R. Gorlin, J. Sauk, H. Sedano, 1977 .

Recurrent aphthous stomatitis. An immunofluorescence study.

R. Gorlin, S. Ullman, 1978, Archives of dermatology.

Growth retardation, alopecia, pseudo-anodontia, and optic atrophy--the GAPO syndrome: report of a patient and review of the literature.

R. Gorlin, R. Tipton, R. Tipton, 1984, American journal of medical genetics.

Psychological Component in the Etiology of Geographic Tongue

R. Gorlin, L. Meskin, R. Redman, 1966, The American journal of psychiatry.

Fibroblast growth factors, their receptors and receptor disorders.

R. Gorlin, 1997, Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery.

Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR

L. Biesecker, C. Tifft, A. Wilkie, 2004, Nature Genetics.

Thoma's Oral Pathology.

R. Gorlin, H. Goldman, W. Hurt, 1972, Journal of periodontology.

Bowen's disease of the mucous membrane of the mouth; a review of the literature and a presentation of six cases.

R. Gorlin, 1950, Oral surgery, oral medicine, and oral pathology.

NATAL AND NEONATAL TEETH: FOLKLORE AND FACT.

R. Gorlin, J. Bodenhoff, 1963, Pediatrics.

Frontonasal dysplasia (median cleft face syndrome): comments on etiology and pathogenesis.

R. Gorlin, M. Cohen, H. Sedano, 1971, Birth defects original article series.

Syndromes of the Head and Neck

Robert J. Gorlin, R. Gorlin, M. Cohen, 1976 .

Familial occurrence of mesiodens.

R. Gorlin, H. Sedano, 1969, Oral surgery, oral medicine, and oral pathology.

Achondrogenesis within the scope of connately manifested generalized skeletal dysplasias

R. Gorlin, P. Maroteaux, W. Remagen, 1974, Zeitschrift für Kinderheilkunde.

Dyssegmental dwarfism. A lethal anisospondylic camptomicromelic dwarfism.

R. Gorlin, L. Langer, J. Gruhn, 1978, American journal of diseases of children.

Reiter's syndrome

R. Gorlin, J. Pindborg, G. Asboe-hansen, 1963 .

Stapes fixation and proximal symphalangism

R. Gorlin, J. Wolfson, G. Kietzer, 2004, Zeitschrift für Kinderheilkunde.

Minor orofacial abnormalities in an Eskimo population.

R. Gorlin, A. Jarvis, 1972, Oral surgery, oral medicine, and oral pathology.

Multiple mucosal neuromas, pheochromocytoma, medullary carcinoma of the thyroid and marfanoid body build with muscle wasting

R. Gorlin, B. Mirkin, 1972, Zeitschrift für Kinderheilkunde.

Odontogenic tumors. Classification, histopathology, and clinical behavior in man and domesticated animals

R. Gorlin, J. Pindborg, Robert J. Gorlin, 1961, Cancer.

An unusual odontogenic tumor. Report of a case.

R. Gorlin, A. Chaudhry, R. Vickers, 1962, Oral surgery, oral medicine, and oral pathology.

ODONTOGENIC TUMORS IN MAN AND ANIMALS: PATHOLOGIC CLASSIFICATION AND CLINICAL BEHAVIOR—A REVIEW *

R. Gorlin, L. Meskin, R. Brodey, 1963, Annals of the New York Academy of Sciences.

Submandibular salivary gland sialoliths perforated through the oral floor.

R. Gorlin, N. Holte, M. El Deeb, 1981, Oral surgery, oral medicine, and oral pathology.

The genetic aspects of facial abnormalities.

R. Gorlin, W. S. Boggs, 1977, Advances in human genetics.

Mannosidosis: Clinical, Morphologic, Immunologic, and Biochemical Studies

R. Desnick, R. Gorlin, R. Brunning, 1976, Pediatric Research.

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.

C Eng, K. Lunetta, C. Romano, 1999, Human molecular genetics.

Beryllium rickets: its effect on the teeth, the mandibular joint, and the bones of the skull of the albino rat.

R. Gorlin, 1951, Oral surgery, oral medicine, and oral pathology.

Further delineation of the branchio-oculo-facial syndrome.

H. Brunner, R. Gorlin, A. Lin, 1995, American journal of medical genetics.

Cutis laxa. A manifestation of generalized elastolysis.

R. Gorlin, R. Goltz, A. Hult, 1965 .

Multiple nevoid basal cell carcinoma, odontogenic keratocysts and skeletal anomalies. A syndrome.

R. Gorlin, J. Yunis, N. Tuna, 1963, Acta dermato-venereologica.

Oral mucosal involvement in nevus unius lateris (ichthyosis hystrix).

R. Gorlin, H. Brown, 1960, Archives of dermatology.

Four hereditary mucosal syndromes: comparative histology and exfoliative cytology of Darier-White's disease, hereditary benign intraepithelial dyskeratosis, white sponge nevus, and pachyonychia congenita.

R. Gorlin, C. Witkop, 1961, Archives of dermatology.

Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease

R. Gorlin, G. Diaz, S. Taniuchi, 2003, Nature Genetics.

Oral disease in man and animals based on analysis of 1,135 cases in a variety of species.

W. C. Peterson, R. Gorlin, 1967, Archives of dermatology.

Multiple hamartoma syndrome (Cowden disease).

R. Gorlin, W. Gentry, N. R. Eskritt, 1974, Archives of dermatology.

Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease.

M. Nelen, H. Kremer, J. Fryns, 1997, Human molecular genetics.

CUTIS LAXA—A MANIFESTATION OF GENERALIZED ELASTOLYSIS

R. Gorlin, R. Goltz, A. Hult, 1966 .

The Face in the Diagnosis of Dysmorphogenesis

R. Gorlin, H. Sedano, W. S. Boggs, 1975 .

The oral manifestations of cyclic (periodic) neutropenia. Does periadenitis mucosa necrotica recurrens (Sutton) exist? A need for reevaluation.

R. Gorlin, A. Chaudhry, 1960, Archives of dermatology.

Nevoid Basal‐Cell Carcinoma Syndrome

Robert J. Gorlin, R. Gorlin, 1987, Medicine.

Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome

J. Yunis, R. Gorlin, 2004, Chromosoma.

POSSIBLE ANALOGOUS CUTANEOUS AND ODONTOGENIC TUMORS.

W. C. Peterson, R. Gorlin, 1964, Archives of dermatology.

Neurocutaneous Disorders: Nevoid basal cell carcinoma (Gorlin) syndrome

R. Gorlin, 2004 .

11 – Clinical Manifestations of Chromosome Disorders

R. Gorlin, 1974 .

The Effect of Anticonvulsant Drugs Upon the Gingiva—A Series of Analyses of 1048 Patients

R. Gorlin, J. Bearman, D. F. Mitchell, 1960 .

The oral manifestations of cyclopia. Review of the literature and report of two cases.

R. Gorlin, H. Sedano, 1963, Oral surgery, oral medicine, and oral pathology.

Leukonychia totalis, multiple sebaceous cysts and renal calculi: a syndrome.

R. Gorlin, L. L. Bushkell, G. Jensen, 1975, Birth defects original article series.

A two-hit model for developmental defects in Gorlin syndrome

R. Gorlin, S. Levanat, J. Fantasia, 1996, Nature Genetics.

Popliteal pterygium syndrome . A syndrome comprising cleft lip-palate, popliteal and intercrural pterygia, digital and genital anomalies.

R. Gorlin, J. Červenka, H. Sedano, 1968, Pediatrics.

Nevoid basal cell carcinoma (Gorlin) syndrome: unanswered issues.

R. Gorlin, 1999, The Journal of laboratory and clinical medicine.

Nevoid basal cell carcinoma syndrome.

R. Gorlin, 1995, Dermatologic clinics.

Warty Dyskeratoma: A Note Concerning Its Occurrence on the Oral Mucosa

W. C. Peterson, R. Gorlin, 1967 .

Ectopic sebaceous glands of the tongue.

R. Gorlin, J. Trodahl, L. Albjerg, 1967, Archives of dermatology.

Intraoral minor salivary gland tumors: An analysis of 1,414 cases

R. Gorlin, A. Chaudhry, R. Vickers, 1961 .

Congenital localized absence of skin and associated abnormalities resembling epidermolysis bullosa. A new syndrome.

V. Anderson, R. Gorlin, F. Lynch, 1966, Archives of dermatology.

Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts

J. Murray, H. van Bokhoven, R. Gorlin, 2002, Journal of medical genetics.

Carcinoma of the antrum: a clinical and histopathologic study.

R. Gorlin, A. Chaudhry, D. Mosser, 1960, Oral surgery, oral medicine, and oral pathology.

Calcifying odontogenic cyst. Range, variations and neoplastic potential.

R. Gorlin, F. Praetorius, E. Hjørting-Hansen, 1981, Acta odontologica Scandinavica.

The calcifying odontogenic cyst--a possible analogue of the cutaneous calcifying epithelioma of Malherbe. An analysis of fifteen cases.

R. Gorlin, J. Pindborg, R. Vickers, 1962, Oral surgery, oral medicine, and oral pathology.

International collaborative study on ghost cell odontogenic tumours: calcifying cystic odontogenic tumour, dentinogenic ghost cell tumour and ghost cell odontogenic carcinoma.

R. Gorlin, M. Altini, M. Shear, 2008, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

Ameloblastoma: Delineation of early histopathologic features of neoplasia

R. Gorlin, R. Vickers, Robert J. Gorlin, 1970, Cancer.

The calcifying odontogenic cyst. A new entity and possible analogue of the cutaneous calcifying epithelioma of malherbe

R. Gorlin, L. S. Hansen, J. Pindborg, 1964, Cancer.

Potentialities of oral epithelium manifest by mandibular dentigerous cysts.

R. Gorlin, 1957, Oral surgery, oral medicine, and oral pathology.

Usher's syndrome type III.

R. Gorlin, S. Feinstein, A. J. Duvall, 1979, Archives of otolaryngology.

Multiple glomus tumor of the pseudocavernous hemangioma type; report of case manifesting a dominant inheritance pattern.

R. Gorlin, R. Fusaro, J. Benton, 1960, Archives of dermatology.

The Effect of Vitamin a Deficiency Upon Experimental Oral Carcinogenesis

N. Rowe, R. Gorlin, 1959, Journal of dental research.

Genetic and Metabolic Deafness

B. Konigsmark, R. Gorlin, 1976 .

Confirmation of the Yemenite (Warburg) deaf-blind hypopigmentation syndrome.

R. Hennekam, R. Gorlin, 1996, American journal of medical genetics.

The ermine phenotype: pigmentary-hearing loss heterogeneity.

R. Gorlin, N. O'Doherty, 1988, American journal of medical genetics.

The characteristic dentition of incontinentia pigmenti.

J. Anderson, R. Gorlin, John A. Anderson, 1960, The Journal of pediatrics.

Multiple mucosal neuromas, pheochromocytoma and medullary carcinoma of the thyroid—a syndrome

R A Vickers, R. Gorlin, J. Červenka, 1968, Cancer.

Malignant melanoma of the oral cavity. Report of a case.

R. Gorlin, A. Chaudhry, R. Burke, 1960, Oral surgery, oral medicine, and oral pathology.

Chromosomal Abnormalities and Oral Anomalies

R. Gorlin, 1963, American journal of surgery.

CHROMOSOMAL ABNORMALITIES AND ORAL ANOMALIES.

R. Gorlin, Robert S. Redman, Robert J. Gorlin, 1964, Journal of dental research.

Warburg syndrome: lethal neurodysplasia with autosomal recessive inheritance.

R. Gorlin, T. Thompson, C. Whitley, 1983, The Journal of pediatrics.

Effect of X-Chromosome Aneuploidy on Jaw Growth

R. Gorlin, R. Redman, B. Shapiro, 1965, Journal of dental research.

Orodigitofacial dysostosis--a new syndrome. A study of 22 cases.

R. Gorlin, J. Psaume, 1962, The Journal of pediatrics.

Hypertrophied Frenuli, Oligophrenia, Familial Trembling and Anomalies of the Hand

V. Anderson, R. Gorlin, C. Scott, 1961 .

Stomatologic aspects of cutaneous diseases. Incontinentia pigmenti.

R. Gorlin, H. Sedano, 1978, The Journal of dermatologic surgery and oncology.

Systemic Inherited Disorders with Dental Involvement

R. Gorlin, J. Sauk, H. Sedano, 1977 .

Achondrogenesis: new nosology with evidence of genetic heterogeneity.

R. Gorlin, C. Whitley, 1983, Radiology.

Partial trisomy 4q syndrome: Case report and review

R. Gorlin, J. Červenka, Robert J. Gorlin, 1976, Human Genetics.

Deletion of chromosome 4q33 leads to qter. Is it different from 4q31 leads to qter deletion syndrome?

R. Gorlin, M. Tuchman, J. Ebrahimi, 1983, American journal of medical genetics.

Sialolithiasis of a minor salivary gland.

R. Gorlin, A. Chaudhry, D. Reynolds, 1960, Oral surgery, oral medicine, and oral pathology.

Systemic Inherited Disorders with Involvement of Jaw Bones

R. Gorlin, J. Sauk, H. Sedano, 1977 .

LYMPHOEPITHELIAL LESIONS OF THE ORAL CAVITY. REPORT OF FOUR CASES.

R. Gorlin, E. A. Smart, R. Vickers, 1963, Oral surgery, oral medicine, and oral pathology.

Oxyphilic granular cell adenoma (oncocytoma).

R. Gorlin, A. Chaudhry, 1958, Oral surgery, oral medicine, and oral pathology.

Histiocytosis X. Clinical, radiologic, and histologic findings with special attention to oral manifestations.

R. Gorlin, P. Cernea, H. Sedano, 1969, Oral surgery, oral medicine, and oral pathology.

An analysis of oral cytodiagnosis

R. Gorlin, B. Shapiro, 1964, Cancer.

Hypohidrotic ectodermal dysplasia in females

V. Anderson, R. Gorlin, T. Old, 1970, Zeitschrift für Kinderheilkunde.

Papillary cystadenoma of minor salivary gland origin. Report of a case.

R. Gorlin, D. F. Mitchell, A. Chaudhry, 1960, Oral surgery, oral medicine, and oral pathology.

Papillary cystadenoma lymphomatosum (adenolymphoma); a review of the literature.

R. Gorlin, A. Chaudhry, 1958, American journal of surgery.

Minor craniofacial anomalies among a Negro population. II. Prevalence of tongue anomalies.

R. Gorlin, B. Schaumann, F. Peagler, 1970, Oral surgery, oral medicine, and oral pathology.

Minor craniofacial anomalies among a Negro population. I. Prevalence of cleft uvula, commissural lip pits, preauricular pits, torus palatinus, and torus mandibularis.

R. Gorlin, B. Schaumann, F. Peagler, 1970, Oral surgery, oral medicine, and oral pathology.

In memoriam: Jens J. Pindborg, August 17, 1921 to August 6, 1995.

R. Gorlin, F. Praetorius, 1995, Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics.

Variations in Salivary Protein Concentration

R. Gorlin, 1948, Journal of dental research.

Hereditary component in the etiology of benign migratory glossitis.

R. Gorlin, R. Redman, B. Shapiro, 1972, American journal of human genetics.

Incidence of Geographic Tongue among 3,668 Students at the University of Minnesota

R. Gorlin, L. Meskin, R. Redman, 1963, Journal of dental research.

Heterotopic lymphoid tissue; a diagnostic problem.

R. Gorlin, 1957, Oral surgery, oral medicine, and oral pathology.

Spondylocarpotarsal synostosis syndrome (with or without unilateral unsegmented bar).

B. Hamel, R. Gorlin, D. Donnai, 1994, American journal of medical genetics.

Goldenhar complex: a further case with uncommon associated anomalies.

P. Gasparini, R. Gorlin, A. Castriota Scanderbeg, 1997, American journal of medical genetics.

The Malformed Infant and Child: An Illustrated Guide

R. Gorlin, R. Goodman, 1983 .

Robinow (fetal face) syndrome: report of a boy with dominant type and an infant with recessive type.

R. Gorlin, P. Kantaputra, J. Sudasna, 1999, American journal of medical genetics.

Some soft tissue heritable tumors.

R. Gorlin, 1976, Birth defects original article series.

The multiple nevoid basal cell carcinoma syndrome revisited.

R. Gorlin, H. Sedano, 1971, Birth defects original article series.

Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans

Charles E. Schwartz, Eva Morava, Denise Horn, 2003, Nature Genetics.

Systemic Inherited Disorders Associated with Facial Clefting

R. Gorlin, J. Sauk, H. Sedano, 1977 .

Warty dyskeratoma. A note concerning its occurrence on the oral mucosa.

W. C. Peterson, R. Gorlin, 1967, Archives of dermatology.

The tricho-rhino-phalangeal syndrome with exostoses (or Langer-Giedion syndrome): four additional patients without mental retardation and review of the literature.

L. Lutter, R. Laxová, R. Gorlin, 1984, American journal of medical genetics.

Oral cysts containing gastric or intestinal mucosa. An unusual embryological accident or heterotopia.

R. Gorlin, J. Jirásek, 1970, Archives of otolaryngology.

The role of the gingival biopsy in secondary amyloid disease.

R. Gorlin, R. Gottsegen, 1949, Oral surgery, oral medicine, and oral pathology.

No chromosome deletion found on prometaphase banding in two cases of Langer-Giedion syndrome.

R. Gorlin, J. Červenka, L. Langer, 1982, American journal of medical genetics.

Tricho-rhino-phalangeal syndrome.

R. Gorlin, M. Cohen, J. Wolfson, 1969, American journal of diseases of children.

Frontometaphyseal Dysplasia: A New Syndrome

R. Gorlin, M. Cohen, 1969 .

Periarteritis nodosa; report of a case with involvement of the tongue.

R. Gorlin, R. Gottsegen, 1949, Oral surgery, oral medicine, and oral pathology.

Photographic documentation of syndrome diagnosis.

R. Stevenson, J. Allanson, R. Winter, 1997, American journal of medical genetics.

The face in genetic disorders

Robert J. Gorlin, R. Gorlin, Richard M. Goodman, 1970 .

Frontonasal malformation as a field defect and in syndromic associations.

R. Gorlin, H. Sedano, 1988, Oral surgery, oral medicine, and oral pathology.

Odontogenic myxoma: some histochemical considerations.

R. Gorlin, H. Sedano, 1965, Archives of Oral Biology.

Single central incisor in familial holoprosencephaly.

R. Gorlin, M. Pierpont, S. Berry, 1984, The Journal of pediatrics.

The palate and Down's syndrome.

R. Gorlin, R. Redman, B. Shapiro, 1967, The New England journal of medicine.

Measurement of normal and reportedly malformed palatal vaults. II. Normal juvenile measurements.

R. Gorlin, R. Redman, B. Shapiro, 1965, Journal of dental research.

Adams-Oliver syndrome revisited.

R. Gorlin, C. Whitley, Robert J. Gorlin, 1991, American journal of medical genetics.

Solitary maxillary central incisor and short stature.

E. Rappaport, R. Gorlin, A. Lucky, 1977, The Journal of pediatrics.

Measurement of Normal and Reportedly Malformed Palatal Vaults. II. Normal Juvenile Measurements

R. Gorlin, R. Redman, B. Shapiro, 1963 .

Craniotubular bone disorders

R. Gorlin, 2005, Pediatric Radiology.

Structural basis of banding pattern of human chromosomes.

R. Gorlin, J. Červenka, H. L. Thorn, 1973, Cytogenetics and cell genetics.

Syndromes involving the sinuses—Congenital and acquired

R. Gorlin, H. Sedano, 1968 .

Congenital cardiac, pulmonary, and vascular malformations in oculoauriculovertebral dysplasia

J. Moller, R. Gorlin, J. Edwards, 1982, Pediatric Cardiology.

Robin's syndrome. A probably X-linked recessive subvariety exhibiting persistence of left superior vena cava and atrial septal defect.

R. Gorlin, J. Červenka, J. Sauk, 1970, American journal of diseases of children.

Frontonasal dysplasia.

R. Gorlin, M. Cohen, H. Sedano, 1970, Jornal de Pediatria.

Oculo-facio-cardio-dental (OFCD) syndrome.

R. Gorlin, H. Obwegeser, A. Marashi, 1996, American journal of medical genetics.

Further delineation of the C (trigonocephaly) syndrome.

J. Opitz, R. Gorlin, E. McPherson, 1981, American journal of medical genetics.

The Ekman-Westborg-Julin syndrome

S. Kreiborg, R. Gorlin, J. Brinch-Iversen, 1997 .

Clinical homogeneity and genetic heterogeneity in Weill–Marchesani syndrome

A. Munnich, A. Mégarbané, R. Gorlin, 2003, American journal of medical genetics. Part A.

Designation of the TARP syndrome and linkage to Xp11.23‐q13.3 without samples from affected patients

L. Biesecker, R. Gorlin, Kyle T Kurpinski, 2003, American journal of medical genetics. Part A.

Problems in the delineation of pseudotrisomy 13 syndrome: Reply to Drs. Norman, Donnai, Martínez-frías, Urioste, Martin, and Frías

R. Gorlin, M. Cohen, 1992 .

Short arm deletion of chromosome 18 in cebocephaly.

V. Anderson, J. Yunis, R. Gorlin, 1968, American journal of diseases of children.

Patient described by Chun et al. may not present Antley-Bixler syndrome.

R. Gorlin, 1999, American journal of medical genetics.

Melanotic neuroectodermal tumor of infancy‐A neoplasm of neural crest origin. Report of a case associated with high urinary excretion of vanilmandelic acid

R. Gorlin, Kugenio D. Borello, Kugenio D. Borello, 1966, Cancer.

Systemic Inherited Disorders with Oral or Perioral Soft Tissue Involvement

R. Gorlin, J. Sauk, H. Sedano, 1977 .

Cartilage-hair-hypoplasia and Hodgkin disease.

R. Gorlin, 1992, American journal of medical genetics.

Otodental syndrome, oculo-facio-cardio-dental (OFCD) syndrome, and lobodontia: dental disorders of interest to the pediatric radiologist

R. Gorlin, 1998, Pediatric Radiology.

Radiculomegaly of canine teeth and congenital cataracts: confirmation of a syndrome.

R. Gorlin, A. Marashi, 1992, American journal of medical genetics.

Radiculomegaly of canines and congenital cataracts--a syndrome?

R. Gorlin, A. Marashi, 1990, Oral surgery, oral medicine, and oral pathology.

Oligodontia, taurodontia, and sparse hair growth--a syndrome.

R. Gorlin, K. Moller, B. Wedge, 1973, The Journal of speech and hearing disorders.

Oral Manifestations of Inherited Disorders

R. Gorlin, J. Sauk, H. Sedano, 1977 .

Osteoglophonic dysplasia: review and further delineation of the syndrome.

M. Keogh, R. Gorlin, Q. Qazi, 1996, American journal of medical genetics.

Craniofacial manifestations of Ehlers-Danlos syndromes, cutis laxa syndromes, and cutis laxa-like syndromes.

R. Gorlin, M. Cohen, 1989, Birth defects original article series.

Blepharo-cheilo-dontic (BCD) syndrome.

R. Gorlin, E. Zackai, H. Wiedemann, 1996, American journal of medical genetics.

Direct hyperbilirubinemia and hepatic fibrosis: a new presentation of Jeune syndrome (asphyxiating thoracic dystrophy).

B. Burke, R. Gorlin, S. Schwarzenberg, 1987, American journal of medical genetics. Supplement.

A case simulating hurler syndrome of unusual longevity, without abnormal mucopolysacchariduria: A proposed classification of the various forms of the syndrome and similar diseases

R. Gorlin, R. Kronenberg, L. Langer, 1966 .

Oro-facial-digital syndrome.

R. Gorlin, 1969, Archives of otolaryngology.

Oral-facial-digital syndrome type VI (Váradi syndrome): further clinical delineation.

E. Zackai, R. Gorlin, M. Münke, 1990, American journal of medical genetics.

Histology of early reactions of skin and mucous membrane of the lip of the mouse to a single application of a carcinogen.

R. Gorlin, B. Levy, R. Gottsegen, 1951, Journal of the National Cancer Institute.

The pigmentation of dental tissues in erythropoietic (congenital) porphyria.

R. Gorlin, J. Trodahl, S. Schwartz, 1972, Journal of oral pathology.

Malformation syndromes. A selected miscellany.

R. Gorlin, J. Červenka, K. Moller, 1975, Birth defects original article series.

Trisomy 8 syndrome.

R. Gorlin, C. C. Lai, 1975, Clinical orthopaedics and related research.

Weill-Marchesani syndrome--possible linkage of the autosomal dominant form to 15q21.1.

R. Gorlin, P. Kramer, A. Jahed, 1996, American journal of medical genetics.

Oral manifestations of the Fitzgerald-Gardner, Pringle-Bourneville, Robin. adrenogenital, and Hurler-Pfaundler syndromes.

R. Gorlin, A. Chaudhary, E. Kelln, 1960, Oral surgery, oral medicine, and oral pathology.

Achondroplasia

R. Gorlin, L. Langer, P. A. Baumann, 1968, Clinical pediatrics.

Genetics and periodontal disease.

R. Gorlin, R. Stallard, B. Shapiro, 1967, Journal of periodontology.

Stomatologic aspects of cutaneous diseases. Behçet's syndrome.

R. Gorlin, H. Sedano, 1977, The Journal of dermatologic surgery and oncology.

A nonpathologic allele (IW) for low alpha-L-iduronidase enzyme activity vis-a-vis prenatal diagnosis of Hurler syndrome.

R. Gorlin, W. Krivit, C. Whitley, 1987, American journal of medical genetics.

FOCAL DERMAL HYPOPLASIA SYNDROME.

W. C. Peterson, R. Gorlin, R. Goltz, 1970, Acta dermato-venereologica.

The SHORT syndrome: further delineation and natural history.

R. Gorlin, A. Lipson, C. Cowell, 1989, Journal of medical genetics.

Sebaceous adenoma in a dog.

R. Gorlin, 1957, Oral surgery, oral medicine, and oral pathology.

Tumors of the Buccal and Labial Mucosa

R. Gorlin, 1957, Dental Clinics of North America.

Hereditary dentinogenesis imperfecta.

R. Gorlin, D. F. Mitchell, A. Chaudhry, 1959, The Journal of pediatrics.

TORUS MANDIBULARIS: A GENETICS STUDY.

V. Anderson, R. Gorlin, C. C. Johnson, 1965, American journal of human genetics.

Down syndrome due to partial trisomy 21q

R. Gorlin, J. Červenka, Gholman Reza Djavadi, 1977, Clinical genetics.

Benign neoplastic fibro-osseous lesion of the mandible: report of a case.

R. Gorlin, A. Chaudhry, R. Burke, 1960, Oral surgery, oral medicine, and oral pathology.

Papillary Cystadenoma Lymphomatosum (Adenolymphoma)

R. Gorlin, A. Chaudry, 1958 .

A MORPHOLOGIC STUDY OF A CARCINOGENIC PROCEDURE IN THE HAMSTER SUBMANDIBULAR GLAND.

R. Gorlin, B. Shapiro, 1964, Archives of oral biology.

Hypertelorism, microtia, and facial clefting. A newly described inherited syndrome.

R. Gorlin, D. Bixler, J. C. Christian, 1969, American journal of diseases of children.

The ameloblastoma and the craniopharyngioma; their similarities and differences.

R. Gorlin, A. Chaudhry, 1959, Oral surgery, oral medicine, and oral pathology.

Syndromes of genetic juvenile retinal detachment

R. Gorlin, W. Knobloch, 2004, Zeitschrift für Kinderheilkunde.

Oral melanotic pigmentation in polyostotic fibrous dysplasia, Albright's syndrome.

R. Gorlin, A. Chaudhry, 1957, Oral surgery, oral medicine, and oral pathology.

Pseudo-trisomy 13 syndrome.

R. Gorlin, M. Cohen, M. Michael Cohen, 1991, American journal of medical genetics.

Amyloid-containing odontogenic tumors.

R. Gorlin, D. Dahlin, R. Vickers, 1965, Oral surgery, oral medicine, and oral pathology.

Dermatoglyphics in trisomy 8 mosaicism

R. Gorlin, J. Červenka, B. Schaumann, 2004, Humangenetik.

Trisomy 22 with 'cat eye' anomaly.

R. Gorlin, J. Červenka, R. Franciosi, 1977, Journal of medical genetics.

Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity.

R. Gorlin, A. Richieri‐Costa, 1994, American journal of medical genetics.

Familial reciprocal C/18 translocation.

R. Gorlin, L. Pinsky, A. Digeorge, 1966, American journal of human genetics.

Radiological findings in Hallermann-Streiff syndrome: report of five cases and a review of the literature.

J. Graham, R. Gorlin, A. Aylsworth, 1991, American journal of medical genetics.

Proteus syndrome.

R. Gorlin, 1984, The Journal of clinical dysmorphology.

Double dens invaginatus of molarized maxillary central incisors, premolarization of maxillary lateral incisors, multituberculism of the mandibular incisors, canines and first premolar, and sensorineural hearing loss.

R. Gorlin, P. Kantaputra, 1992, Clinical dysmorphology.

Oral manifestations of systemic genetic disorders. 1.

R. Gorlin, H. Sedano, 1971, Postgraduate medicine.

Oral manifestations of systemic genetic disorders. 4.

R. Gorlin, H. Sedano, 1971, Postgraduate medicine.

G deletion syndromes

R. Gorlin, 1973 .

Inherited multicentric osteolysis with arthritis: a variant resembling Torg syndrome in a Saudi family.

J. Martignetti, R. Desnick, R. Gorlin, 2000, American journal of medical genetics.

The oto-palato-digital syndrome. A new symptom-complex consisting of deafness, dwarfism, cleft palate, characteristic facies, and a generalized bone dysplasia.

R. Gorlin, L. Langer, B. Dudding, 1967, American journal of diseases of children.

Brain anomalies, retardation of mentality and growth, ectodermal dysplasia, skeletal malformations, Hirschsprung disease, ear deformity and deafness, eye hypoplasia, cleft palate, cryptorchidism, and kidney dysplasia/hypoplasia (BRESEK/BRESHECK): new X-linked syndrome?

B. Burke, R. Gorlin, O. Reish, 1997, American journal of medical genetics.

Craniofacial dysostosis, hypertrichosis, genital hypoplasia, ocular, dental, and digital defects: confirmation of the Gorlin-Chaudhry-Moss syndrome.

R. Gorlin, J. B. Bijlsma, P. Ippel, 1992, American journal of medical genetics.

Craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies-a new syndrome?

R. Gorlin, M. L. Moss, A. Chaudhry, 1960, The Journal of pediatrics.

Hereditary hemorrhagic telangiectasia: the Rendu-Weber-Osler syndrome.

R. Gorlin, H. Sedano, 1978, The Journal of dermatologic surgery and oncology.

OCULOAURICULOVERTEBRAL DYSPLASIA.

R. Gorlin, K. Jue, E. Goldschmidt, 1963, The Journal of pediatrics.

Diprosopus, anencephaly, and facial clefting.

R. Gorlin, 1988, American journal of medical genetics.

Hyaline bodies of Rushton. Some histochemical considerations concerning their etiology.

R. Gorlin, H. Sedano, 1968, Oral surgery, oral medicine, and oral pathology.

Blepharo-cheilo-dontic (BCD) syndrome.

E. Zackai, M. Warburg, B. Prahl-Andersen, 2009, American journal of medical genetics.

Developmental anomalies of the jaws.

R. Gorlin, J. Gorlin, 1971, Seminars in roentgenology.

Dyssegmental dwarfism: a new syndrome of lethal dwarfism.

J. Campbell, R. Gorlin, S. Handmaker, 1977, Birth defects original article series.

Frontometaphyseal dysplasia--evidence for X-linked inheritance.

R. Winter, R. Gorlin, 1980, American journal of medical genetics.

A first description of dyssegmental dysplasia.

R. Gorlin, 1987, American journal of medical genetics.

Dyssegmental dwarfism (?s): lethal anisospondylic camptomicromelic dwarfism.

R. Gorlin, L. Langer, 1978, Birth defects original article series.

Complete absence of the permanent dentition: an autosomal recessive disorder.

R. Gorlin, S. Moss, N. Herman, 1980, American journal of medical genetics.

Focal epithelial hyperplasia in an Eskimo population.

R. Gorlin, A. Jarvis, 1972, Oral surgery, oral medicine, and oral pathology.

Benign hemangiopericytoma of dog lip.

R. Gorlin, A. Chaudhry, 1957, Oral surgery, oral medicine, and oral pathology.

Cranio-carpo-tarsal dysplasia or the whistling face syndrome. II. Oral intercommissural distance in children.

R. Gorlin, J. Červenka, P. Figalovã, 1969, American journal of diseases of children.

Plantar lipomatosis, unusual facial phenotype and developmental delay: a new MCA/MR syndrome.

R. Gorlin, M. Pierpont, F. Stewart, 1998, American journal of medical genetics.

Dermatoglyphics in XXYY Klinefelter's syndrome.

R. Gorlin, M. Alter, F. Peagler, 1966, American journal of human genetics.

Stomatologic aspects of cutaneous diseases. Benign mucous membrane pemphigoid.

R. Gorlin, H. Sedano, 1978, The Journal of dermatologic surgery and oncology.

Epidermolysis bullosa.

R. Gorlin, H. Sedano, 1989, Oral surgery, oral medicine, and oral pathology.

OCCURRENCE OF HETEROTOPIC GASTRIC MUCOSA IN THE TONGUE.

R. Gorlin, V. Kalnins, R. Izant, 1964, The Journal of pediatrics.

Gastrointestinal cyst of the tongue: A possible duplication cyst of foregut origin

R. Gorlin, S. Myers, 1997 .

The Dubowitz syndrome: a retrospective.

R. Gorlin, K. Moller, 1985, Journal of craniofacial genetics and developmental biology. Supplement.

Melnick-Needles syndrome in males.

R. Gorlin, M. Krajewska-Walasek, J. Winkielman, 1987, American journal of medical genetics.

The oto-palato-digital syndrome, proposed type II.

R. Gorlin, S. Jéquier, N. Fitch, 1983, American journal of medical genetics.

The oto-palato-digital (OPD) syndrome in females.

A. Poznanski, R. Gorlin, I. Hendon, 1973, Oral surgery, oral medicine, and oral pathology.

X-linked or autosomal dominant, lethal in the male, inheritance of the Melnick-Needles (osteodysplasty) syndrome? A reappraisal.

R. Gorlin, J. Knier, 1982, American journal of medical genetics.

The hand in the oto palato digital syndrome

A. Poznanski, R. Gorlin, R. Macpherson, 1973 .

Oto-palato-digital syndrome.

R. Gorlin, 1967, American journal of diseases of children.

Otopalatodigital syndrome: radiologic findings in the hand and foot.

A. Poznanski, R. Gorlin, S. Garn, 1974, Birth defects original article series.

Inheritance of the oto-palato-digital syndrome.

G. Turner, R. Gorlin, 1970, American journal of diseases of children.

Multiple mucosal neuromas, pheochromocytoma, medullary carcinoma of the thyroid and marfanoid body build with muscle wasting: reexamination of a syndrome of neural crest malmigration.

R. Gorlin, R. Vickers, 1971, Birth defects original article series.

Microcephaly with agenesis of corticospinal tracts and arthrogryposis, hypospadias, single umbilical artery, hypertelorism, and renal and adrenal hypoplasia--previously undescribed syndrome.

R. Gorlin, M. Pierpont, J. Coad, 1997, American journal of medical genetics.

What Syndrome Is This?

R. Gorlin, J. Geiger, Iftikhar Ahmed, 2000, Pediatric dermatology.

Prenatal sex determination. Detection of "Y body".

R. Gorlin, J. Červenka, R. Bendel, 1971, Obstetrics and gynecology.

THE ROLE OF EXFOLIATIVE CYTOLOGY IN ORAL CANCER DETECTION.

R. Gorlin, B. Shapiro, W. Jordan, 1964, Oral surgery, oral medicine, and oral pathology.

Effects of Cortisone on Chemical Carcinogenesis in Hamster Pouch and Submandibular Salivary Gland

R. Gorlin, W. R. Sabes, Robert J. Gorlin, 1963, Journal of dental research.

Primary malignant melanoma of the oral cavity. A review of 105 cases

R. Gorlin, A. Chaudhry, Anna Hampel, 1958, Cancer.

Congenital monostotic fibrous dysplasia--a new possibly autosomal recessive disorder.

R. Gorlin, D. Waite, M. El Deeb, 1979, Journal of oral surgery.

Autosomal dominant cemental dysplasia.

R. Gorlin, H. Sedano, R. Kuba, 1982, Oral surgery, oral medicine, and oral pathology.

Oral manifestations of Crouzon's disease.

R. Gorlin, A. Chaudhry, E. Kelln, 1960, Oral surgery, oral medicine, and oral pathology.

"Newer" facial clefting syndromes.

R. Gorlin, J. Červenka, M. Cohen, 1977, Birth defects original article series.

PTEN mutations and Proteus syndrome

R. Hennekam, R. Winter, C. Eng, 2001, The Lancet.

Oculo-facio-cardio-dental (OFCD) syndrome.

R. Gorlin, H. Obwegeser, 1997, Clinical dysmorphology.

Pyle's disease (familial metaphyseal dysplasia). A presentation of two cases and argument for its separation from craniometaphyseal dysplasia.

R. Gorlin, J. Spranger, M. F. Koszalka, 1970, The Journal of bone and joint surgery. American volume.

Stomatologic aspects of cutaneous diseases. Multiple hamartoma syndrome (Cowden's syndrome).

R. Gorlin, H. Sedano, 1979, The Journal of Dermatologic Surgery and Oncology.

Weill-Marchesani Syndrome in Two Generations: Genetic Heterogeneity or Pseudodominance?

R. Gorlin, I. Shapiro, 1974 .

Frontonasal dysplasia.

R. Gorlin, T. Nagai, H. Sedano, 2020, The Journal of pediatrics.

Stomatologic aspects of cutaneous diseases. Lichen planus.

R. Gorlin, H. Sedano, 1978, The Journal of dermatologic surgery and oncology.

Gardner's syndrome without polyposis?

R. Gorlin, 1968, Humangenetik.

Living history-biography: from oral pathology to craniofacial genetics.

R. Gorlin, 1993, American journal of medical genetics.

The oral manifestation of keratosis follicularis.

R. Gorlin, A. Chaudhry, 1959, Oral surgery, oral medicine, and oral pathology.

Pycnodysostosis: Clinical and Genetic Considerations

V. Anderson, R. Gorlin, H. Sedano, 1968 .

Fluorescing structures of human metaphase chromosomes. Detection of "Y body".

R. Gorlin, J. Červenka, D. E. Jacobson, 1971, American journal of human genetics.

Coeliac disease in twins

R. Gorlin, S. Daack-Hirsch, J. V. Bokhoven, 2002, Journal of medical genetics.

A Histochemical Study of Hamster Submandibular Lesions

R. Gorlin, L. Wattenberg, B. Shapiro, 1966, Journal of dental research.

NATAL AND NEONATAL TEETH

R. Gorlin, J. Bodenhoff, 1963, Pediatrics.

NATAL AND NEONATAL TEETH: FOLKLORE AND FACT.

R. Gorlin, J. Bodenhoff, 1963, Pediatrics.