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J M Opitz

Showing results (251-260 of 338) with videos related to

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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|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.
American Journal of Medical Genetics|February 1, 1983
Differential diagnosis of Nager acrofacial dysostosis syndrome: report of four patients with Nager syndrome and discussion of other related syndromesF Halal, J Herrmann, P D Pallister, et al.
American Journal of Medical Genetics|June 8, 2001
Klippel-Feil anomaly with Sprengel anomaly, omovertebral bone, thumb abnormalities, and flexion-crease changes: novel association or syndrome?A R Larson, K D Josephson, R M Pauli, et al.
Lancet (London, England)|July 10, 1971
Geleophysic dwarfism--a "focal" mucopolysaccharidosis?J W Spranger, E F Gilbert, G A Tuffli, et al.
Pageof 34

Showing results (251-260 of 338) with videos related to

Sort By:
Pageof 34
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|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.
American Journal of Medical Genetics|February 1, 1983
Differential diagnosis of Nager acrofacial dysostosis syndrome: report of four patients with Nager syndrome and discussion of other related syndromesF Halal, J Herrmann, P D Pallister, et al.
American Journal of Medical Genetics|June 8, 2001
Klippel-Feil anomaly with Sprengel anomaly, omovertebral bone, thumb abnormalities, and flexion-crease changes: novel association or syndrome?A R Larson, K D Josephson, R M Pauli, et al.
Lancet (London, England)|July 10, 1971
Geleophysic dwarfism--a "focal" mucopolysaccharidosis?J W Spranger, E F Gilbert, G A Tuffli, et al.
Pageof 34