J. Hall

发表

Folate and its various ramifications.

J. Hall, F. Solehdin, Hall Jg, 1998, Advances in pediatrics.

Clinical, genetic, and epidemiological factors in neural tube defects.

J M Friedman, J. Friedman, J. Hall, 1988, American journal of human genetics.

The impact of birth defects and genetic diseases.

J. Hall, 1997, Archives of pediatrics & adolescent medicine.

International Nosology of Heritable Disorders of Connective Tissue, Berlin, 1986.

D. Sillence, J. Opitz, P. Beighton, 1988, American journal of medical genetics.

A recessive form of congenital contractures and torticollis associated with malignant hyperthermia.

U. Froster-Iskenius, J. Hall, J. Waterson, 1988, Journal of medical genetics.

A pattern of craniofacial and limb defects secondary to aberrant tissue bands.

K. Jones, D. W. Smith, A. Ebbin, 1974, The Journal of pediatrics.

Perinatal and first year follow‐up of patients with Prader‐Willi syndrome: normal size of hands and feet

M. Hayden, D. Chitayat, B. McGillivray, 1989, Clinical genetics.

Autosomal dominant inheritance of endocardial cushion defect.

J. Hall, S. O'Nualláin, S. Stamm, 1977, Birth defects original article series.

Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus and postaxial polydactyly--a new syndrome? Part I: clinical, causal, and pathogenetic considerations.

S. Clarren, S. Reed, J. Hall, 1980, American journal of medical genetics.

Review and hypotheses: somatic mosaicism: observations related to clinical genetics.

J. Hall, J. Hall, 1988, American journal of human genetics.

The importance of the fetal origins of adult disease for geneticists

J. Hall, Jg Hall, 2007, Clinical genetics.

Multiple congenital anomalies associated with oral anticoagulants.

J. Hall, W. Shaul, J. Hall, 1977, American journal of obstetrics and gynecology.

Embryologic development and monozygotic twinning.

J. Hall, E. Lopez-Rangel, 1996, Acta geneticae medicae et gemellologiae.

Twins and twinning.

J. Hall, Judith G. Hall, 1996, American journal of medical genetics.

Dominant distal arthrogryposis in a Maori family with marked variability of expression.

J. Hall, P. Klemp, 1995, American journal of medical genetics.

Thanatophoric dysplasia and cloverleaf skull.

M. Golabi, S. Kottamasu, J. Hall, 1987, American journal of medical genetics. Supplement.

The phenotypic variability of diastrophic dysplasia.

D. Rimoin, F. Skovby, J. Hall, 1978, The Journal of pediatrics.

Limb pterygium syndromes: a review and report of eleven patients.

S. Reed, Harold Chen, J. Hall, 1982, American journal of medical genetics.

Familial renal hypophosphatemia, minor facial anomalies, intracerebral calcifications, and non-rachitic bone changes: apparently new syndrome?

D. Chitayat, O. Flodmark, B. McGillivray, 1990, American journal of medical genetics.

Genomic imprinting: nature and clinical relevance.

J. Hall, 1997, Annual review of medicine.

Thrombocytopenia and absent radius (TAR) syndrome.

J. Hall, 1987, Journal of medical genetics.

Molecular nosology of heritable disorders of connective tissue.

P. Beighton, R. Pyeritz, A. De Paepe, 1992, American journal of medical genetics.

Three distinct types of X‐linked arthrogryposis seen in 6 families

S. Reed, J. Hall, C. Scott, 1982, Clinical genetics.

Analysis of Pena Shokeir phenotype.

J. Hall, J. Reynolds, John M. Opitz, 1986, American journal of medical genetics.

The distal arthrogryposes: delineation of new entities--review and nosologic discussion.

S. Reed, J. Hall, G. Greene, 1982, American journal of medical genetics.

Familial essential ("benign") chorea.

T. Bird, J. Hall, C. Carlson, 1976, Journal of medical genetics.

The value of the study of natural history in genetic disorders and congenital anomaly syndromes.

J. Hall, Judith G. Hall, 1988, Journal of medical genetics.

Twinning: mechanisms and genetic implications.

J. Hall, Judith G. Hall, 1996, Current opinion in genetics & development.

Lymphedema in Noonan syndrome: Clues to pathogenesis and prenatal diagnosis and review of the literature

J. Opitz, H. Hoyme, J. Fryns, 1987, American journal of medical genetics.

Noonan phenotype associated with neurofibromatosis.

J. Opitz, J. Allanson, M. V. Van Allen, 1985, American journal of medical genetics.

How imprinting is relevant to human disease.

J. Hall, Judith G. Hall, 1990, Development (Cambridge, England). Supplement.

Juvenile galactosialidosis in a white male: a new variant.

D. Chitayat, J. Dimmick, J. Hall, 1988, American journal of medical genetics.

Embryopathy associated with oral anticoagulant therapy.

J. Hall, 1976, Birth defects original article series.

Chondrodysplasia punctata and maternal warfarin use during pregnancy.

J. Hall, H. Emery, W. Shaul, 1975, American journal of diseases of children.

Additional information on familial essential (benign) chorea

T. Bird, J. Hall, 1978, Clinical genetics.

A new form of autosomal dominant arthrogryposis.

J. Hall, A. Berry, M. Lai, 1991, Journal of medical genetics.

Part I. Amyoplasia: a common, sporadic condition with congenital contractures.

S. Reed, J. Hall, E. P. Driscoll, 1983, American journal of medical genetics.

Small structural changes of chromosome 8

H. Hoehn, J. Hall, J. Hanson, 1977, Human Genetics.

No evidence for chromosomal mosaicism in multiple tissues of 10 patients with 45 XO Turner syndrome

J. Callis, H. Hoehn, J. Burns, 1979, Clinical genetics.

Human diseases and genomic imprinting.

J. Hall, 1999, Results and problems in cell differentiation.

Genomic Imprinting

J. Hall, 1996, Nature Medicine.

Bleeding diathesis in Noonan syndrome: a common association.

J. Opitz, J. Allanson, A. Zipursky, 1988, American journal of medical genetics.

Vitamin A teratogenicity.

J. Hall, 1984, The New England journal of medicine.

Osteogenesis imperfecta type II delineation of the phenotype with reference to genetic heterogeneity.

D. Sillence, D. Rimoin, J. Hall, 1984, American journal of medical genetics.

Amyoplasia, the most common type of arthrogryposis: the potential for good outcome.

K. Jaffe, J. Hall, J. Sells, 1996, Pediatrics.

The Jeune syndrome (asphyxiating thoracic dystrophy) in an adult.

H. Kaplan, J. Friedman, J. Hall, 1975, The American journal of medicine.

ACHOO syndrome (autosomal dominant compelling helio-ophthalmic outburst syndrome).

R. Pagon, J. Hall, W. R. Collie, 1978, Birth defects original article series.

Apparent postnatal onset of some manifestations of the Wiedemann-Beckwith syndrome.

D. Chitayat, J. Friedman, R. Couch, 1990, American journal of medical genetics.

Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly--a new syndrome? Part II: Neuropathological considerations.

E. Alvord, S. Clarren, J. Hall, 1980, American journal of medical genetics.

Mosaicism in pseudoachondroplasia.

J. Hecht, J. Hall, M. Deere, 1997, American journal of medical genetics.

Nontraditional inheritance.

J. Hall, K. D. Austin, Katherine Duffin Austin, 1992, Pediatric clinics of North America.

X-linked cutis laxa: defective cross-link formation in collagen due to decreased lysyl oxidase activity.

P. Byers, K. Holbrook, P. Bornstein, 1980, The New England journal of medicine.

Non-traditional forms of inheritance in skeletal dysplasias

J. Hall, E. Lopez-Rangel, 2005, Pediatric Radiology.

Bone dysplasias, nontraditional mechanisms of inheritance and monozygotic twins

J. Hall, E. Lopez-Rangel, 1997, Pediatric Radiology.

Multifactorial inheritance of non‐syndromic macrocephaly

J. Hall, F. Fraser, G. Watters, 1996, Clinical genetics.

Arthrogryposis associated with unsuccessful attempts at termination of pregnancy.

J. Hall, 1996, American journal of medical genetics.

Genomic imprinting and its clinical implications.

J. Hall, 1992, The New England journal of medicine.

Genetic aspects of arthrogryposis.

J. Hall, 1985, Clinical orthopaedics and related research.

Obstetric and Gynecologic Problems in Women With Chondrodystrophies

J. Allanson, J. Hall, 1986, Obstetrics and gynecology.

Prometaphase chromosomes in five patients with the Brachmann-de Lange syndrome.

C. Disteche, J. Hall, H. Thuline, 1981, American journal of medical genetics.

Acromesomelic dwarfism: manifestations in childhood.

E. Franken, J. Dorst, R. K. Beals, 1977, American journal of medical genetics.

Errors of morphogenesis: concepts and terms. Recommendations of an international working group.

J. Opitz, K. Benirschke, J. Hall, 1982, The Journal of pediatrics.

DIASTROPHIC DWARFISM

V. McKusick, J. Hall, C. Scott, 1972, Medicine.

Neuroleptic Malignant Syndrome (NMS): What are the Genetic Factors?

J. Hall, S. Bamforth, 1987, Canadian journal of psychiatry. Revue canadienne de psychiatrie.

Teratogens associated with congenital contractures in humans and in animals.

S. Reed, J. Hall, 1982, Teratology.

Chromosome maps of man and mouse. IV

M. Lyon, J. Edwards, V. Buckle, 1989, Annals of human genetics.

Vitamin A: a newly recognized human teratogen. Harbinger of things to come?

J. Hall, 1984, The Journal of pediatrics.

Tuberous sclerosis: case report and investigation of family members.

R. D. Wilson, J. Hall, B. McGillivray, 1985, Canadian Medical Association journal.

Encephalocraniocutaneous lipomatosis. Report of two cases and a review of the literature.

D. Chitayat, V. Riccardi, J. Friedman, 1989, Neurofibromatosis.

Lethal respiratory course and additional features expand the phenotypic spectrum of PIEZO2‐related distal arthrogryposis type 5

A. Synnes, A. Barnicoat, C. Longman, 2022, American journal of medical genetics. Part A.

Congenital rubella syndrome associated with calcific epiphyseal stippling and peroxisomal dysfunction.

H. Dunn, J. Chantler, A. Tingle, 1990, The Journal of pediatrics.

New syndrome of chronic mucocutaneous candidiasis.

J. Hall, J. Chandler, K. Rodaway, 1977, Birth defects original article series.

Prenatal diagnosis of congenital bullous ichthyosiform erythroderma (epidermolytic hyperkeratosis) by fetal skin biopsy.

R. Filly, R. Sagebiel, M. Golbus, 1980, The New England journal of medicine.

Apnea and sudden unexpected death in infants with achondroplasia.

K. Jones, D. Rimoin, M. Partington, 1984, The Journal of pediatrics.

Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs.

D. Chitayat, R. Couch, J. Hall, 1990, American journal of medical genetics.

Maternal and fetal sequelae of anticoagulation during pregnancy.

R. Pauli, J. Hall, K. M. Wilson, 1980, The American journal of medicine.

Problems in diagnosing neurofibromatosis.

A. Knudson, T. Fitzpatrick, J. Mulvihill, 1981, Advances in neurology.

Turner syndrome and its variants.

D. Gilchrist, J. Hall, J G Hall, 1990, Pediatric clinics of North America.

Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes.

R. Pagon, H. Hoehn, T. Norwood, 1979, American journal of human genetics.

Genomic imprinting: review and relevance to human diseases.

J. Hall, J. Hall, 1990, American journal of human genetics.

Standard growth curves for achondroplasia.

J. Rotter, D. Rimoin, J. Hall, 1978, The Journal of pediatrics.

Association of amyoplasia with gastroschisis, bowel atresia, and defects of the muscular layer of the trunk.

J. Carey, C. Curry, F. Greenberg, 1986, American journal of medical genetics.

Chromosomal abnormalities associated with congenital contractures (arthrogryposis)

C. Timmons, S. Reed, A. Aylsworth, 1985, Clinical genetics.

U-P-what?

J. Hall, 1999, The Journal of pediatrics.

Growth curves for height for diastrophic dysplasia, spondyloepiphyseal dysplasia congenita, and pseudoachondroplasia.

D. Rimoin, R. Pyeritz, J. Hall, 1982, American journal of diseases of children.

The lethal multiple pterygium syndromes.

J. Hall, J. Hall, 1984, American journal of medical genetics.

Body wall defects with reduction limb anomalies: a report of fifteen cases.

R. Pagon, J. Siebert, J. Hall, 1979, Birth defects original article series.

Comments on the Neu-Laxova syndrome and CAD complex.

S. Reed, C. Curry, K. Laurence, 1981, American journal of medical genetics.

Pediatric Diseases and Epigenetics

J. Hall, 2016 .

More on marker X chromosomes, mental retardation and macro-orchidism.

P. Jacobs, H. Hoehn, E. Rudak, 1979, The New England journal of medicine.

The use of radiographic visualization for prenatal diagnosis.

G. Omenn, J. Hall, L. Karp, 1977, Birth defects original article series.

Uterine structural anomalies and arthrogryposis—death of an urban legend

J. Hall, 2013, American journal of medical genetics. Part A.

A lethal neonatal dwarfing condition with short ribs, polysyndactyly, cranial synostosis, cleft palate cardiovascular and urogenital anomalies and severe ossification defect.

D. Hickok, J. Hall, L. Karp, 1977, Teratology.

Arthrogryposis multiplex congenita: etiology, genetics, classification, diagnostic approach, and general aspects.

J. Hall, J. Hall, 1997, Journal of pediatric orthopedics. Part B.

Brief clinical report: an unusual bandlike web in an infant with lethal multiple pterygium syndrome.

U. Froster-Iskenius, C. Curry, J. Hall, 1988, American journal of medical genetics.

Risks to sibs of probands with neural tube defects: data for clinic populations in British Columbia.

A. Sadovnick, B. Keena, J. Hall, 1986, American journal of medical genetics.

An approach to congenital contractures (arthrogryposis).

J. Hall, 1981, Pediatric annals.

Mouse homologues of human hereditary disease.

J. Edwards, J. Hall, A. Searle, 1994, Journal of medical genetics.

Review and hypothesis: Syndromes with severe intrauterine growth restriction and very short stature—Are they related to the epigenetic mechanism(s) of fetal survival involved in the developmental origins of adult health and disease?

Judith G Hall, J. Hall, J. Hall, 2010, American journal of medical genetics. Part A.

Prenatal genetic diagnosis and elective abortion in women over 35: utilization and relative impact on the birth prevalence of Down syndrome in Washington State.

D. Luthy, H. Hoehn, J. Hall, 1980, American journal of medical genetics.

Achondroplasia—a genetic and statistical survey

K. K. Smith, H. Abbey, J. Hall, 1970, Annals of human genetics.

Gonadal mosaicism in pseudoachondroplasia.

V. McKusick, J. Dorst, J. Hall, 1987, American journal of medical genetics.

Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1

E. Mickelson, B. McGillivray, J. Hall, 2006, Journal of Medical Genetics.

Microphallus, growth hormone deficiency, and hypoglycemia in Russell-Silver syndrome.

J. Hall, 1978, A M A Journal of Diseases of Children.

Three-generation dominant transmission of the Silver-Russell syndrome.

J. Hall, L. Shapiro, P. A. Duncan, 1990, American journal of medical genetics.

Unilateral disomy as a possible explanation for Russell-Silver syndrome.

J. Hall, 1990, Journal of medical genetics.

Angelman ' s syndrome , abnormality of 15 qll-13 , and imprinting

J. Hall, 2004 .

Association between age of onset and parental inheritance in Huntington chorea.

J. Hall, L. Te-Juatco, 1983, American journal of medical genetics.

The frequency and financial burden of genetic disease in a pediatric hospital.

J. Opitz, J. Hall, E. Powers, 1978, American journal of medical genetics.

1995 ASHG presidential address. The challenges and opportunities of times of change.

J. Hall, 1996, American journal of human genetics.

Genomic imprinting: summary of an NICHD conference.

Golder N Wilson, J. Hall, G. Wilson, 1993, American journal of medical genetics.

Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome.

D. Chitayat, B. Keena, J. Friedman, 1989, American journal of medical genetics.

The radiologic assessment of short stature--dwarfism.

J. Dorst, J. Hall, C. Scott, 1972, Radiologic clinics of North America.

Familial asymmetric crying facies. Its occurrence secondary to hypoplasia of the anguli oris depressor muscles.

J. Hall, M. Miller, M. Miller, 1979, American journal of diseases of children.

Thrombocytopenia with absent radius.

J. Hall, 1977, Archives of disease in childhood.

Gardner syndrome and periampullary malignancy.

R. Pauli, J. Hall, J. Hall, 1980, American journal of medical genetics.

Part II. Amyoplasia: twinning in amyoplasia--a specific type of arthrogryposis with an apparent excess of discordantly affected identical twins.

S. Reed, D. Weaver, A. Schinzel, 1983, American journal of medical genetics.

Lip pits, cleft lip and/or palate, and congenital heart disease.

R. Pauli, J. Hall, 1980, American journal of diseases of children.

A retrospective study of pregnancy complications among 828 cases of arthrogryposis.

J. Hall, M. Fahy, 1990, Genetic counseling.

Noonan syndrome: the changing phenotype.

Judith G. Hall, J. Opitz, J. Allanson, 1985, American journal of medical genetics.

Dominantly inherited renal adysplasia.

J. Carey, R. Pauli, E. McPherson, 1987, American journal of medical genetics.

Guidelines for human gene nomenclature. An international system for human gene nomenclature (ISGN, 1987).

H. Willard, N. Morton, M. Skolnick, 1987, Cytogenetics and cell genetics.

The 2p partial trisomy syndrome.

J. Hall, C. Dolan, 1977, American journal of diseases of children.

Lower limb anomalies in the thrombocytopenia absent-radius (TAR) syndrome.

J. Hall, A. Sommer, R. Ray, 1980, American journal of medical genetics.

De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome.

D. Chitayat, J. Rootman, D. Kalousek, 1989, American journal of medical genetics.

Majewski osteodysplastic primordial dwarfism type II (MOPD II): Natural history and clinical findings

R. Pauli, J. Hall, C. Scott, 2004, American journal of medical genetics. Part A.

Possible maternal and hormonal factors in neurofibromatosis.

J. Hall, 1981, Advances in neurology.

Neurofibromatosis I: predicting the relation of gene structure to gene function.

J. Allanson, J. Hall, 1991, American journal of medical genetics.

Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposis.

J. Fryns, J. Hall, C. Höweler, 1993, Journal of medical genetics.

Kyphosis in achondroplasia: probably preventable.

J. Hall, 1988, The Journal of pediatrics.

Poland anomaly—report of an unusual family

S. Shalev, J. Hall, 2003, American journal of medical genetics. Part A.

Joubert's syndrome associated with congenital ocular fibrosis and histidinemia.

D. Chitayat, R. Appleton, J. Hall, 1989, Archives of neurology.

Rothmund-Thomson syndrome with severe dwarfism.

R. Pagon, J. Hall, K. M. Wilson, 1980, American journal of diseases of children.

Medial-approach open reduction of hip dislocation in amyoplasia-type arthrogryposis.

K. Jaffe, L. Staheli, J. Hall, 1996, Journal of pediatric orthopedics.

Prenatal diagnosis of genetic osteochondrodysplasias.

J. Hall, W. Horton, C. Scott, 1983, American journal of medical genetics.

The Stickler syndrome presenting as a dominantly inherited cleft palate and blindness.

J. Hall, H. Herrod, 1975, Journal of medical genetics.

Achondroplasia: unexpected familial recurrence.

R. Pauli, J. Hall, C. Reiser, 1984, American journal of medical genetics.

Apert's acrocephalosyndactyly in mother and daughter: cleft palate in the mother.

J. Hall, K. Roberts, 1971, Birth defects original article series.

Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome).

H. Hoehn, J. Hall, M. Jennings, 1980, American journal of medical genetics.

When is careless conception a form of child abuse? Lessons from maternal phenylketonuria.

J. Hall, 2000, The Journal of pediatrics.

Use of genetic counselling services for neural tube defects.

A. Sadovnick, B. Keena, J. Hall, 1987, American journal of medical genetics.

A bone is not a bone is not a bone.

J. Hall, 1998, The Journal of pediatrics.

Familial bilateral antecubital pterygia with severe renal involvement in nail‐patella syndrome

L. Pavone, R. Rizzo, J. Hall, 1993, Clinical genetics.

Partial deletion of the short arm of chromosome 3 (3p25 → 3pter) Further delineation of the clinical phenotype

J. Hall, D. Witt, Brian Biedermann, 1985, Clinical genetics.

Genetic counseling for adoptees at risk for specific inherited disorders.

G. Omenn, J. Hall, K. D. Hansen, 1980, American journal of medical genetics.

Electron microscopy as an aid to diagnosis of disorders of the extracellular matrix: a new type of spondyloepiphyseal dysplasia.

P. Byers, K. Holbrook, P. Bornstein, 1978, Birth defects original article series.

Fetal mortality in sibships of cases with neural tube defects

A. Sadovnick, B. Keena, J. Hall, 1986, Clinical genetics.

Could acrocallosal syndrome and Greig syndrome affect the same developmental gene?

J. Hall, 1990, American journal of medical genetics.

Dominantly inherited ptosis, strabismus and ectopic pupils

J. Hall, E. McPherson, Christine Robertson, 1976, Clinical genetics.

False negative results in patients with fra(X) (q) mental retardation taking oral vitamin supplements.

U. Froster-Iskenius, C. Curry, J. Hall, 1987, The New England journal of medicine.

Difficulties in the classification of the epiphyseal dysplasias.

D. Rimoin, J. Hall, C. Scott, 1975, Birth defects original article series.

Familial insertional translocation of a portion of 3q into 11q resulting in duplication and deletion of region 3q22.1 leads to q24 in different offspring.

J. Hall, R. Williamson, H. Thuline, 1981, American journal of medical genetics.

Fibrodysplasia ossificans progressiva (myositis ossificans progressiva) treatment with disodium etidronate.

L. Staheli, J. Hall, J. Schaller, 1979, Jornal de Pediatria.

Orthopaedic Aspects of the Trismus Pseudocamptodactyly Syndrome

S. Tredwell, J. Hall, P. Gropper, 1984, Journal of pediatric orthopedics.

A new arthrogryposis syndrome with facial and limb anomalies.

W. Truog, J. Hall, D. Plowman, 1975, American journal of diseases of children.

Segregation analysis of microcephaly.

A. Chakravarti, C. Aston, B. McGillivray, 1996, American journal of medical genetics.

An approach to research on congenital contractures.

J. Hall, 1984, Birth defects original article series.

The early history of Pallister-Hall syndrome-Buried treasure of a sort.

J. Hall, 2016, Gene.

Hydrocephalus, agyria, retinal dysplasia, encephalocele (HARD +/- E) syndrome: an autosomal recessive condition.

R. Pagon, S. Clarren, J. Hall, 1978, Birth defects original article series.

Head growth in achondroplasia: use of ultrasound studies.

J. Hall, W. Horton, C. Scott, 1982, American journal of medical genetics.

Cultural influences and neural tube defects in the East Indian Sikh population of British Columbia.

B. Keena, J. Hall, M. Jawanda, 1987, Birth defects original article series.

Conditional overdominance at an alcohol dehydrogenase locus in yeast.

C. Wills, J. Hall, 1987, Genetics.

Functional alcohol dehydrogenase mutants of Saccharomyces cerevisiae conferring temperature-conditional allyl alcohol resistance.

C. Wills, J. Hall, 1987, Genetics.

Clinical course and systemic correlates of retinopathy of prematurity in quintuplets.

J. Kylstra, S. Freedman, J. Hall, 1995, American journal of ophthalmology.

Normal male carriers in the fra(X) form of X-linked mental retardation (Martin-Bell syndrome).

U. Froster-Iskenius, B. McGillivray, J. Hall, 1986, American journal of medical genetics.

Failure to early prenatal diagnosis in classic achondroplasia.

R. Filly, D. Luthy, R. Pagon, 1979, American journal of medical genetics.

Risks of anticoagulation during pregnancy.

R. Pauli, J. Hall, K. M. Wilson, 1980, American heart journal.

Morphogenesis: Re: Clinical, natural history, and imaging information on patients included in reports

R. Stevenson, J. Graham, H. Hoyme, 2003, American journal of medical genetics. Part A.

Growth curves for height in Noonan syndrome

J E Allanson, J. Allanson, B. Keena, 1986, Clinical genetics.

Noonan syndrome-an unusual family with above average intelligence, a high incidence of cancer and rare type of vasculitis.

J. Hall, M. Berberich, 1976, Birth defects original article series.

Re: Majewski osteodysplastic primordial dwarfism type II (MOPD II) complicated by stroke: Clinical report and review of cerebral vascular anomalies [Brancati et al., 2005: Am J Med Genet 139A:212–215]

J. Hall, 2006, American Journal of Medical Genetics. Part A.

New mechanisms for genetic disease and nontraditional modes of inheritance.

S. Langlois, J. Hall, E. Lopez-Rangel, 1995, Advances in pediatrics.

Inbreeding and population dynamics of the Chillingham cattle (Bos taurus)

S. Hall, J. Hall, 1988 .

The natural history of achondroplasia.

J. Hall, J. Hall, 1988, Basic life sciences.

The adaptation of enzymes to temperature: catalytic characterization of glucosephosphate isomerase homologues isolated from Mytilus edulis and Isognomon alatus, bivalve molluscs inhabiting different thermal environments.

J. Hall, 1985, Molecular biology and evolution.

See One, Do One, Teach One

J. Hall, J G Hall, 1999, Pediatrics.

Autosomal recessive acrocephalosyndactyly revisited.

S. Reed, J. Hall, J. Hanson, 1980, American journal of medical genetics.

The Summitt syndrome: observations on a third case.

J. Hall, J. Hanson, C. Sells, 1979, American journal of medical genetics.

Amniotic fluid cell mosaicism for presumptive trisomy 20

D. Luthy, H. Hoehn, T. Norwood, 1978, Clinical genetics.

Prenatal diagnosis of chromosomal mosaicism for trisomy D.

H. Hoehn, J. Hall, F. Dill, 1977, The Journal of pediatrics.

Posterolateral (Bochdalek's) diaphragmatic hernia in sisters.

J. Hall, L. Pollack, 1979, American journal of diseases of children.

New Mitochondrial Disease Identified In Monozygotic Twin Boys

V. Jobanputra, R. Happle, B. Gelb, 2023, American journal of medical genetics. Part A.

Hypoplastic left heart in a patient with 45,X/46,XX/47,XXX mosaicism.

J. Hall, N. Talner, Y. Hsia, 1978, American journal of medical genetics.

Short-limbed dwarfism: ultrasonographic diagnosis by mensuration of fetal femoral length.

R. Filly, J. Carey, M. Golbus, 1981, Radiology.

Report from the workshop on Pallister-Hall syndrome and related phenotypes.

L. Biesecker, J. Graham, A. Verloes, 1996, American journal of medical genetics.

Coarctation of the aorta in male cousins with similar maternal environmental exposure to insect repellent and insecticides.

J. McLaughlin, J. Hall, S. Stamm, 1975, Pediatrics.

A syndrome characterized by contractures and pterygia of upper body associated with umbilical hernia, short stature, and distinctive face in an Arabic family

R. Spiegel, S. Shalev, J. Hall, 2005, American journal of medical genetics. Part A.

The new genetics and its relevance to orthopedics.

J. Hall, 1991, Clinical orthopaedics and related research.