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E H Zackai

Showing results (1-10 of 179) with videos related to

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American Journal of Medical Genetics|August 17, 1999
Deletion 4q34.2E H Zackai
American Journal of Medical Genetics|April 1, 1988
Gene location in neurofibromatosisD Stambolian, E H Zackai
Teratology|August 1, 1994
Unusual craniofacial dysmorphia due to prenatal alcohol and cocaine exposureN H Robin, E H Zackai
Cytogenetics and Cell Genetics|January 1, 1973
Ring chromosome 7 with variable phenotypic expressionE H Zackai, W R Breg
American Journal of Human Genetics|October 30, 1998
A new twist: some patients with Saethre-Chotzen syndrome have a microdeletion syndromeE H Zackai, C A Stolle
American Journal of Medical Genetics|January 1, 1980
Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunctionE H Zackai, B S Emanuel
American Journal of Medical Genetics|March 17, 1997
Circumferential ringed creases ("Michelin tire babies") with specific histologic findings and/or karyotype abnormalities: clues to molecular pathogenesis?R E Schnur, E H Zackai
American Journal of Medical Genetics|August 1, 1988
Holoprosencephaly: association with interstitial deletion of 2p and review of the cytogenetic literatureM Münke, B S Emanuel, E H Zackai
The Journal of Pediatrics|June 1, 1982
Congenital hydronephrosis, skeletal dysplasia, and severe developmental retardation: the Schinzel-Giedion syndromeR I Kelley, E H Zackai, E B Charney
American Journal of Medical Genetics|May 8, 2000
Craniosynostosis: molecular testing-a necessity for counselingE H Zackai, K W Gripp, C A Stolle
Pageof 18

Showing results (1-10 of 179) with videos related to

Sort By:
Pageof 18
American Journal of Medical Genetics|August 17, 1999
Deletion 4q34.2E H Zackai
American Journal of Medical Genetics|April 1, 1988
Gene location in neurofibromatosisD Stambolian, E H Zackai
Teratology|August 1, 1994
Unusual craniofacial dysmorphia due to prenatal alcohol and cocaine exposureN H Robin, E H Zackai
Cytogenetics and Cell Genetics|January 1, 1973
Ring chromosome 7 with variable phenotypic expressionE H Zackai, W R Breg
American Journal of Human Genetics|October 30, 1998
A new twist: some patients with Saethre-Chotzen syndrome have a microdeletion syndromeE H Zackai, C A Stolle
American Journal of Medical Genetics|January 1, 1980
Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunctionE H Zackai, B S Emanuel
American Journal of Medical Genetics|March 17, 1997
Circumferential ringed creases ("Michelin tire babies") with specific histologic findings and/or karyotype abnormalities: clues to molecular pathogenesis?R E Schnur, E H Zackai
American Journal of Medical Genetics|August 1, 1988
Holoprosencephaly: association with interstitial deletion of 2p and review of the cytogenetic literatureM Münke, B S Emanuel, E H Zackai
The Journal of Pediatrics|June 1, 1982
Congenital hydronephrosis, skeletal dysplasia, and severe developmental retardation: the Schinzel-Giedion syndromeR I Kelley, E H Zackai, E B Charney
American Journal of Medical Genetics|May 8, 2000
Craniosynostosis: molecular testing-a necessity for counselingE H Zackai, K W Gripp, C A Stolle
Pageof 18