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M Opitz

Showing results (361-370 of 520) with videos related to

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Birth Defects Original Article Series|January 1, 1974
Pathology of chondrodysplasia punctata rhizomelic typeC Viseskul, J M Opitz, J W Spranger, et al.
American Journal of Medical Genetics|January 1, 1980
Cerebroarthrodigital syndrome: a newly recognized formal genesis syndrome in three patients with apparent arthromyodysplasia and sacral agenesis, brain malformation and digital hypoplasiaJ W Spranger, A Schinzel, T Myers, et al.
Journal of Cutaneous Pathology|January 1, 1974
Cutis marmorata telangiectatica congenitaB H Way, J Herrmann, E F Gilbert, et al.
American Journal of Medical Genetics. Part A|July 29, 2003
Splenogonadal fusion-limb defect "syndrome" and associated malformationsFiona McPherson, Jaime L Frias, Diane Spicer, et al.
American Journal of Medical Genetics|October 21, 1999
Trisomy 2p syndrome: a fetus with anencephaly and postaxial polydactylyG K Hahm, R F Barth, G M Schauer, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1977
Sudden infant death due to congenital adrenal hypoplasiaM A Russell, J M Opitz, C Viseskul, et al.
Lancet (London, England)|April 24, 1976
Letter: Developmental mixoploidy and trisomy-20 syndromeL F Meissner, P D Pallister, S L Inhorn, et al.
Birth Defects Original Article Series|January 1, 1993
Developmental abnormalities resulting in short umbilical cordE Gilbert-Barness, R M Drut, R Drut, et al.
The Journal of Pediatrics|September 1, 1971
I-cell disease: a clinical pictureJ G Leroy, J W Spranger, M Feingold, et al.
Zeitschrift Fur Kinderheilkunde|August 31, 1973
Familial bilateral renal agenesis and hereditary renal adysplasiaR M Buchta, C Viseskul, E F Gilbert, et al.
Pageof 52

Showing results (361-370 of 520) with videos related to

Sort By:
Pageof 52
Birth Defects Original Article Series|January 1, 1974
Pathology of chondrodysplasia punctata rhizomelic typeC Viseskul, J M Opitz, J W Spranger, et al.
American Journal of Medical Genetics|January 1, 1980
Cerebroarthrodigital syndrome: a newly recognized formal genesis syndrome in three patients with apparent arthromyodysplasia and sacral agenesis, brain malformation and digital hypoplasiaJ W Spranger, A Schinzel, T Myers, et al.
Journal of Cutaneous Pathology|January 1, 1974
Cutis marmorata telangiectatica congenitaB H Way, J Herrmann, E F Gilbert, et al.
American Journal of Medical Genetics. Part A|July 29, 2003
Splenogonadal fusion-limb defect "syndrome" and associated malformationsFiona McPherson, Jaime L Frias, Diane Spicer, et al.
American Journal of Medical Genetics|October 21, 1999
Trisomy 2p syndrome: a fetus with anencephaly and postaxial polydactylyG K Hahm, R F Barth, G M Schauer, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1977
Sudden infant death due to congenital adrenal hypoplasiaM A Russell, J M Opitz, C Viseskul, et al.
Lancet (London, England)|April 24, 1976
Letter: Developmental mixoploidy and trisomy-20 syndromeL F Meissner, P D Pallister, S L Inhorn, et al.
Birth Defects Original Article Series|January 1, 1993
Developmental abnormalities resulting in short umbilical cordE Gilbert-Barness, R M Drut, R Drut, et al.
The Journal of Pediatrics|September 1, 1971
I-cell disease: a clinical pictureJ G Leroy, J W Spranger, M Feingold, et al.
Zeitschrift Fur Kinderheilkunde|August 31, 1973
Familial bilateral renal agenesis and hereditary renal adysplasiaR M Buchta, C Viseskul, E F Gilbert, et al.
Pageof 52