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J M Opitz

Showing results (171-180 of 338) with videos related to

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European Journal of Pediatrics|May 1, 1980
The ECP syndrome, another autosomal dominant cause of monodactylous ectrodactylyJ M Opitz, J L Frias, M M Cohen
Postgraduate Medicine|July 1, 1979
Genetic causes and workup of male and female infertility. 3. Details of the clinical evaluationJ M Opitz, S S Shapiro, D T Uehling
American Journal of Medical Genetics|March 21, 1998
Complete absence or deficiency of one half of the bodyA Carranza, E Gilbert-Barness, F Madrigal, et al.
Lancet (London, England)|May 11, 1974
Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndromeM Lubinsky, J Herrmann, A L Kosseff, et al.
Birth Defects Original Article Series|January 1, 1987
Pathology of chromosome abnormalities in the fetus--pathologic markersE F Gilbert, S Arya, R Laxova, et al.
Birth Defects Original Article Series|January 1, 1975
The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomaliesJ Herrmann, P D Pallister, W Tiddy, et al.
American Journal of Medical Genetics|April 17, 1998
Errors of morphogenesis and developmental field theoryM L Martínez-Frías, J L Frías, J M Opitz
American Journal of Medical Genetics|October 1, 1984
Sensorineural deafness in the FG syndrome: report on four new casesG Neri, B Blumberg, P V Miles, et al.
The New England Journal of Medicine|March 9, 1972
The Stickler syndromeJ M Opitz, T France, J Herrmann, et al.
European Journal of Pediatrics|July 1, 1981
Niemann-Pick disease type C. Pathological, histochemical, ultrastructural and biochemical studiesE F Gilbert, J Callahan, C Viseskul, et al.
Pageof 34

Showing results (171-180 of 338) with videos related to

Sort By:
Pageof 34
European Journal of Pediatrics|May 1, 1980
The ECP syndrome, another autosomal dominant cause of monodactylous ectrodactylyJ M Opitz, J L Frias, M M Cohen
Postgraduate Medicine|July 1, 1979
Genetic causes and workup of male and female infertility. 3. Details of the clinical evaluationJ M Opitz, S S Shapiro, D T Uehling
American Journal of Medical Genetics|March 21, 1998
Complete absence or deficiency of one half of the bodyA Carranza, E Gilbert-Barness, F Madrigal, et al.
Lancet (London, England)|May 11, 1974
Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndromeM Lubinsky, J Herrmann, A L Kosseff, et al.
Birth Defects Original Article Series|January 1, 1987
Pathology of chromosome abnormalities in the fetus--pathologic markersE F Gilbert, S Arya, R Laxova, et al.
Birth Defects Original Article Series|January 1, 1975
The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomaliesJ Herrmann, P D Pallister, W Tiddy, et al.
American Journal of Medical Genetics|April 17, 1998
Errors of morphogenesis and developmental field theoryM L Martínez-Frías, J L Frías, J M Opitz
American Journal of Medical Genetics|October 1, 1984
Sensorineural deafness in the FG syndrome: report on four new casesG Neri, B Blumberg, P V Miles, et al.
The New England Journal of Medicine|March 9, 1972
The Stickler syndromeJ M Opitz, T France, J Herrmann, et al.
European Journal of Pediatrics|July 1, 1981
Niemann-Pick disease type C. Pathological, histochemical, ultrastructural and biochemical studiesE F Gilbert, J Callahan, C Viseskul, et al.
Pageof 34