John M. Opitz

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Cyclopia and cebocephaly in two newborn infants with unbalanced segregation of a familial translocation rcp (1;7)(q32;q34).

A. Schinzel, A. Schinzel, John M. Opitz, 1984, American journal of medical genetics.

Extensions to pedigree analysis. IV. Covariance components models for multivariate traits.

K. Lange, M. Boehnke, John M. Opitz, 1983, American journal of medical genetics.

Emotional symptoms in Prader-Willi syndrome adolescents.

P. Accardo, B. Whitman, J. Reynolds, 1987, American journal of medical genetics.

Screening of mentally retarded males for macro-orchidism and the fragile X chromosome.

P. Howard‐Peebles, W. Finley, John M. Opitz, 1983, American journal of medical genetics.

The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers.

G. Turner, R. Brookwell, A. Daniel, 1983, American journal of medical genetics.

A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation.

M. Pembrey, K. Davies, R. Winter, 1985, American journal of medical genetics.

Interstitial deletion of the long arm of chromosome 10: Del(10)(q11.2q21)

J. Reynolds, John M. Opitz, J. Holden, 1985 .

Microcephaly: genetic counselling and antenatal diagnosis after the birth of an affected child.

J. Tolmie, M. McNay, J. M. Connor, 1987, American journal of medical genetics.

X-linked mental retardation associated with bilateral clasp thumb anomaly.

F. Gareis, J. Mason, John M. Opitz, 1984, American journal of medical genetics.

X-linked mental retardation.

M. G. Blymina, John M. Opitz, Gillian Turner, 1980, American journal of medical genetics.

Genetics of red cell COMT activity: analysis of thermal stability and family data.

R. Weinshilboum, R. Spielman, John M. Opitz, 1981, American journal of medical genetics.

Familial occurrence of hemifacial microsomia with radial limb defects.

S. Clarren, J. Moeschler, John M. Opitz, 1982, American journal of medical genetics.

Dyggve-Melchior-Clausen syndrome: genetic studies and report of affected sibs.

C. Dietrich, P. A. Mourão, S. Toledo, 1979, American journal of medical genetics.

Psychological aspects of genetic counseling. III. Management of guilt and shame.

S. Kessler, P. Ward, H. Kessler, 1984, American journal of medical genetics.

A five-generation family with sacral agenesis and spina bifida: possible similarities with the mouse T-locus.

R. Elston, M. Fellous, F. Demenais, 1982, American journal of medical genetics.

del(20p) with manifestations of arteriohepatic dysplasia.

J. Friedman, J. Byrne, M. Harrod, 1986, American journal of medical genetics.

Tracheal agenesis and associated malformations: a comparison with tracheoesophageal fistula and the VACTERL association.

C. Greenberg, J. Evans, J. Reggin, 1985, American journal of medical genetics.

The fragile X syndrome II: preliminary data on growth and development in males.

M. Partington, John M. Opitz, J. M. Opitz, 1984, American journal of medical genetics.

Therapeutic effects of a ketogenic diet in Rett syndrome.

D. Trauner, R. Haas, T. Merritt, 1986, American journal of medical genetics. Supplement.

Amnion rupture sequence in previable fetuses.

D. Kalousek, S. Bamforth, J. Reynolds, 1988, American journal of medical genetics.

GAPO syndrome (McKusick 23074)--a connective tissue disorder: report on two affected sibs and on the pathologic findings in the older.

J. Opitz, B. Mendonca, M. Sotto, 1990, American journal of medical genetics.

Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes.

E. Zackai, H. Moser, A. Moser, 1986, American journal of medical genetics.

Analysis of Pena Shokeir phenotype.

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

Neu-Laxova syndrome: two further case reports and comments on proposed subclassification.

R. Winter, R. Mueller, C. Naylor, 1983, American journal of medical genetics.

Congenital contractures, edema, hyperkeratosis, and intrauterine growth retardation: a fatal syndrome in Hutterite and Mennonite kindreds.

R. Lowry, K. Morgan, D. Mayock, 1985, American journal of medical genetics.

Folic acid treatment in males and females with fragile-(X)-syndrome.

U. Froster-Iskenius, E. Schwinger, R. Matthes, 1986, American journal of medical genetics.

Autosomal dominant late adult spinal muscular atrophy, type Finkel.

A. Richieri‐Costa, A. Rogatko, O. Frota-Pessoa, 1981, American journal of medical genetics.

Age-of-onset heterogeneity in Huntington disease families.

M. Pericak-Vance, R. Elston, P. Conneally, 1983, American journal of medical genetics.

A lethal autosomal recessive syndrome of multiple congenital contractures.

R. Herva, P. Kirkinen, U. Seppänen, 1985, American journal of medical genetics.

3-M syndrome.

John M. Opitz, D. B. Flannery, J. M. Opitz, 1989, American journal of medical genetics.

Vertical transmission of the neurofibromatosis/Noonan syndrome.

E. McPherson, T. Quattrin, T. Putnam, 1987, American journal of medical genetics.

Evidence that the "neurofibromatosis-Noonan syndrome" is a variant of von Recklinghausen neurofibromatosis.

P. Meinecke, J. Reynolds, John M. Opitz, 1987, American journal of medical genetics.

Selective termination of multiple gestations.

M. Golbus, J. Goldberg, P. Callen, 1988, American journal of medical genetics.

Differential diagnosis of hydrops fetalis.

G. Machin, John M. Opitz, 1981, American journal of medical genetics.

Computerized tomography of the foramen magnum: achondroplastic values compared to normal standards.

C. Mehringer, D. Rimoin, R. Pauli, 1985, American journal of medical genetics.

The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.

T. Gollop, L. Fontes, J. Reynolds, 1985, American journal of medical genetics.

On the statistical determination of major gene mechanisms in continuous human traits: regressive models.

G. Bonney, G E Bonney, J. Reynolds, 1984, American journal of medical genetics.

The perlman syndrome: Familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies

John M. Opitz, M. Martini‐Neri, Giovanni Neri, 2013, American journal of medical genetics.

RSH (so-called Smith-Lemli-Opitz) syndrome.

J. Opitz, John M. Opitz, 1999, Current opinion in pediatrics.

Invited editorial comment: Study of minor anomalies in childhood malignancy

John M. Opitz, 1985, European Journal of Pediatrics.

NOR activity and centromere suppression related in a de novo fusion tdic(9;13)(p22;p13) chromosome in a child with del(9p) syndrome.

J. Opitz, A. Daniel, J. Fitzgerald, 1985, American journal of medical genetics.

New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement--the CFC syndrome.

J. Opitz, J. Carey, G. Neri, 1986, American journal of medical genetics.

The neurofibromatosis-Noonan syndrome.

J. Opitz, D. Weaver, Weaver Dd, 1985, American journal of medical genetics.

Monozygotic twins discordant for trisomy 21.

J. Opitz, L. Voullaire, J. Rogers, 1982, American journal of medical genetics.

Editorial comment on the papers by Hersh et al and Kaplan et al on sternal cleft

J. Opitz, John M. Opitz, 1985 .

Microcephaly: general considerations and aids to nosology.

J. Opitz, M. C. Holt, John M. Opitz, 1990, Journal of craniofacial genetics and developmental biology.