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American Journal of Medical Genetics|February 1, 1987
Presymptomatic testing for Huntington chorea: guidelines for moral and social accountabilityJ F Smurl, D D WeaverAmerican Journal of Medical Genetics|April 1, 1986
Subclavian artery supply disruption sequence: hypothesis of a vascular etiology for Poland, Klippel-Feil, and Möbius anomaliesJ N Bavinck, D D WeaverClinical Genetics|March 1, 1978
Phenotypic and genetic analysis of the silver-Russell syndromeV Escobar, S Gleiser, D D WeaverJournal of Medical Genetics|June 4, 1998
49,XXXXY: a distinct phenotype. Three new cases and reviewJ Peet, D D Weaver, G H VanceAmerican Journal of Medical Genetics|January 10, 1997
Molecular cytogenetic identification of four X chromosome duplicationsA Zhang, D D Weaver, C G PalmerAmerican Journal of Diseases of Children (1960)|April 1, 1986
Analysis of growth in the VATER associationC L Mapstone, D D Weaver, P L YuAmerican Journal of Medical Genetics|February 27, 2001
Distal 13q Deletion Syndrome and the VACTERL association: case report, literature review, and possible implicationsL E Walsh, G H Vance, D D WeaverAmerican Journal of Medical Genetics|February 13, 1995
Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndromeP G Wheeler, D D Weaver, C G PalmerAmerican Journal of Medical Genetics|February 1, 1989
Holoprosencephaly, ear abnormalities, congenital heart defect, and microphallus in a patient with 11q- mosaicismR A Helmuth, D D Weaver, E R WillsPageof 8