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J M Opitz

Showing results (211-220 of 338) with videos related to

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Progress in Clinical and Biological Research|January 1, 1985
The Perlman syndrome: clinical and biological aspectsG Neri, M E Martini-Neri, J M Opitz, et al.
Human Genetics|December 1, 1986
Severe short-limb dwarfism resembling Grebe chondrodysplasiaA S Teebi, S A Al-Awadi, J M Opitz, et al.
American Journal of Medical Genetics|July 27, 2001
Evidence for the "midline" hypothesis in associated defects of laterality formation and multiple midline anomaliesE Gilbert-Barness, D Debich-Spicer, M M Cohen, et al.
American Journal of Medical Genetics. Supplement|January 1, 1986
Two sporadic cases of amelia/phocomelia with similar phenotype: rare and unusually symmetrical form of FFU dysostosis or separate entity?N B Kardon, L P Dana, J M FitzGerald, et al.
Birth Defects Original Article Series|January 1, 1978
Follow-up on a human X-autosome translocation first studied in 1963 and 1964J M Opitz, R I DeMars, S L Inhorn, et al.
European Journal of Pediatrics|March 18, 1977
Absence of spermatogonia in the Prader-Willi syndromeM L Katcher, G J Bargman, E F Gilbert, et al.
European Journal of Pediatrics|April 6, 1976
Studies of malformation syndromes of man XXXXIA: anatomical studies in the Hanhart syndrome--a pathogenetic hypothesisE T Bersu, J C Pettersen, W J Charboneau, et al.
American Journal of Medical Genetics|February 1, 1982
Phenotypic effects of inherited balanced translocationZ Ying, C Zaiyu, L Chunyun, et al.
Birth Defects Original Article Series|January 1, 1978
Diagnostic/genetic studies in severe mental retardationJ M Opitz, E G Kaveggia, M V Durkin-Stamm, et al.
American Journal of Medical Genetics|August 1, 1985
An X-linked recessive basal ganglia disorder with mental retardationR Laxova, E S Brown, K Hogan, et al.
Pageof 34

Showing results (211-220 of 338) with videos related to

Sort By:
Pageof 34
Progress in Clinical and Biological Research|January 1, 1985
The Perlman syndrome: clinical and biological aspectsG Neri, M E Martini-Neri, J M Opitz, et al.
Human Genetics|December 1, 1986
Severe short-limb dwarfism resembling Grebe chondrodysplasiaA S Teebi, S A Al-Awadi, J M Opitz, et al.
American Journal of Medical Genetics|July 27, 2001
Evidence for the "midline" hypothesis in associated defects of laterality formation and multiple midline anomaliesE Gilbert-Barness, D Debich-Spicer, M M Cohen, et al.
American Journal of Medical Genetics. Supplement|January 1, 1986
Two sporadic cases of amelia/phocomelia with similar phenotype: rare and unusually symmetrical form of FFU dysostosis or separate entity?N B Kardon, L P Dana, J M FitzGerald, et al.
Birth Defects Original Article Series|January 1, 1978
Follow-up on a human X-autosome translocation first studied in 1963 and 1964J M Opitz, R I DeMars, S L Inhorn, et al.
European Journal of Pediatrics|March 18, 1977
Absence of spermatogonia in the Prader-Willi syndromeM L Katcher, G J Bargman, E F Gilbert, et al.
European Journal of Pediatrics|April 6, 1976
Studies of malformation syndromes of man XXXXIA: anatomical studies in the Hanhart syndrome--a pathogenetic hypothesisE T Bersu, J C Pettersen, W J Charboneau, et al.
American Journal of Medical Genetics|February 1, 1982
Phenotypic effects of inherited balanced translocationZ Ying, C Zaiyu, L Chunyun, et al.
Birth Defects Original Article Series|January 1, 1978
Diagnostic/genetic studies in severe mental retardationJ M Opitz, E G Kaveggia, M V Durkin-Stamm, et al.
American Journal of Medical Genetics|August 1, 1985
An X-linked recessive basal ganglia disorder with mental retardationR Laxova, E S Brown, K Hogan, et al.
Pageof 34