Gorlin Rj

发表

Holoprosencephaly and facial dysmorphia: nosology, etiology and pathogenesis.

Cohen Mm, Jirăsek Je, Guzman Rt, 1971 .

The multiple nevoid basal cell carcinoma syndrome revisited.

Gorlin Rj, Sedano Ho, 1971 .

The pathology of ameloblastomas and its relationship to treatment.

Gorlin Rj, 1970 .

Cytogenetics and somatic cell genetics: the impact of chromosome banding.

Campbell Ja, Gorlin Rj, Handmaker Sd, 1977 .

Some soft tissue heritable tumors.

Gorlin Rj, 1976 .

Oral cysts containing gastric or intestinal mucosa: unusual embryologic accident or heterotopia.

Jirăsek Je, Gorlin Rj, 1970 .

Focal palmoplantar and marginal gingival hyperkeratosis--a syndrome.

Gorlin Rj, 1976 .

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

Cohen Mm, Gorlin Rj, 1989 .

Hereditary hearing loss associated with musculoskeletal malformations.

Gorlin Rj, 1980 .

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

M. Eldeeb, Waite De, Gorlin Rj, 1979 .

Thoughts on some new and old bone dysplasias.

Gorlin Rj, 1982 .

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.

Gorlin Rj, Kantaputra Pn, 1992 .

Polysplenia syndrome with skeletal and central nervous system anomalies.

Gorlin Rj, Burke Ba, Pantke Oa, 1975 .

Conjoined acardiac monsters.

Gorlin Rj, Amatuzio Jc, 1981 .

Cleft palate, stapes fixation and oligodontia--a new autosomal recessively inherited syndrome.

Gorlin Rj, Paparella Mm, Schlorf Ra, 1971 .

Periapical fibrous dysplasis (cementoma).

Gorlin Rj, Chaudhry Ap, Spink Jh, 1958 .

Facial clefting and its syndromes.

S. Pruzansky, R. Gorlin, J. Červenka, 1971, Birth defects original article series.

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

Gorlin Rj, Vickers Ra, 1971, Birth defects original article series.

Clinical identification of a human equivalent to the short ear (se) murine phenotype.

A. Toutain, D. Lacombe, J. Battin, 1994, Annales de genetique.

Thoma's Oral Pathology.

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