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J M Opitz

Showing results (321-330 of 338) with videos related to

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Birth Defects Original Article Series|January 1, 1987
The value of examining spontaneously aborted human embryos and placentasH J Bruyere, S Arya, J S Kozel, et al.
The Journal of Pediatrics|January 1, 1982
Errors of morphogenesis: concepts and terms. Recommendations of an international working groupJ Spranger, K Benirschke, J G Hall, et al.
American Journal of Medical Genetics|April 1, 1984
Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomaliesB R Elejalde, J M Opitz, M M de Elejalde, et al.
American Journal of Medical Genetics|February 5, 1998
Smith-Lemli-Opitz syndrome in JapanM Tsukahara, K Fujisawa, K Yamamoto, et al.
Clinical Genetics|May 11, 1975
Familial Kallmann syndrome with unilateral renal aplasiaJ D Wegenke, D T Uehling, J B Wear, et al.
Human Genetics|January 1, 1981
The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical pictureA Schinzel, W Schmid, M Fraccaro, et al.
Lancet (London, England)|February 9, 1974
Letter: Parana hard-skin syndrome: study of seven familiesI Cat, N I Magdalena, L P Marinoni, et al.
American Journal of Human Genetics|August 27, 1998
Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domainK Gaudenz, E Roessler, N Quaderi, et al.
American Journal of Medical Genetics|January 1, 1981
Further delineation of the C (trigonocephaly) syndromeR M Antley, D S Hwang, W Theopold, et al.
Clinical Genetics|January 1, 1972
Juvenile GM 1 gangliosidosis: clinical, pathological, chemical and enzymatic studiesJ S O'Brien, M W Ho, M L Veath, et al.
Pageof 34

Showing results (321-330 of 338) with videos related to

Sort By:
Pageof 34
Birth Defects Original Article Series|January 1, 1987
The value of examining spontaneously aborted human embryos and placentasH J Bruyere, S Arya, J S Kozel, et al.
The Journal of Pediatrics|January 1, 1982
Errors of morphogenesis: concepts and terms. Recommendations of an international working groupJ Spranger, K Benirschke, J G Hall, et al.
American Journal of Medical Genetics|April 1, 1984
Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomaliesB R Elejalde, J M Opitz, M M de Elejalde, et al.
American Journal of Medical Genetics|February 5, 1998
Smith-Lemli-Opitz syndrome in JapanM Tsukahara, K Fujisawa, K Yamamoto, et al.
Clinical Genetics|May 11, 1975
Familial Kallmann syndrome with unilateral renal aplasiaJ D Wegenke, D T Uehling, J B Wear, et al.
Human Genetics|January 1, 1981
The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical pictureA Schinzel, W Schmid, M Fraccaro, et al.
Lancet (London, England)|February 9, 1974
Letter: Parana hard-skin syndrome: study of seven familiesI Cat, N I Magdalena, L P Marinoni, et al.
American Journal of Human Genetics|August 27, 1998
Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domainK Gaudenz, E Roessler, N Quaderi, et al.
American Journal of Medical Genetics|January 1, 1981
Further delineation of the C (trigonocephaly) syndromeR M Antley, D S Hwang, W Theopold, et al.
Clinical Genetics|January 1, 1972
Juvenile GM 1 gangliosidosis: clinical, pathological, chemical and enzymatic studiesJ S O'Brien, M W Ho, M L Veath, et al.
Pageof 34