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American Journal of Medical Genetics|February 7, 1998
Heterotaxia in a fetus with campomelia, cervical lymphocele, polysplenia, and multicystic dysplastic kidneys: expanding the phenotype of Cumming syndromeJ E Ming, D M McDonald-McGinn, R I Markowitz, et al.American Journal of Medical Genetics|February 1, 1988
Reproductive risks for carriers of complex chromosome rearrangements: analysis of 25 familiesJ L Gorski, M L Kistenmacher, H H Punnett, et al.Journal of Medical Genetics|July 1, 1994
Paternal transmission of congenital myotonic dystrophyJ Bergoffen, J Kant, J Sladky, et al.American Journal of Medical Genetics|May 1, 1987
Melnick-Needles syndrome in males: a lethal multiple congenital anomalies syndromeA E Donnenfeld, K A Conard, N S Roberts, et al.American Journal of Medical Genetics. Part A|June 3, 2015
Fetal akinesia deformation sequence due to a congenital disorder of glycosylationRebecca Ganetzky, Kosuke Izumi, Andrew Edmondson, et al.Ophthalmic Genetics|September 3, 2010
A case report of a patient with Pfeiffer syndrome, an FGRF 2 mutation (Trp290Cys) and unique ocular anterior segment findingsGerard P Barry, Betina Mucha-Le Ny, Elaine H Zackai, et al.Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|April 26, 2016
Ocular findings associated with chromosome 22q11.2 duplicationBrian J Forbes, Donna M McDonald-McGinn, Georgia Wootton, et al.American Journal of Medical Genetics. Part A|November 11, 2003
Coloboma and other ophthalmologic anomalies in Kabuki syndrome: distinction from charge associationJeffrey E Ming, Karen L Russell, Lynn Bason, et al.American Journal of Medical Genetics|October 1, 1991
Oculodentodigital dysplasia syndrome associated with abnormal cerebral white matterD H Gutmann, E H Zackai, D M McDonald-McGinn, et al.American Journal of Human Genetics|November 1, 1995
Physical mapping of the holoprosencephaly critical region in 18p11.3J Overhauser, H F Mitchell, E H Zackai, et al.Pageof 63