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Scientific Reports|March 21, 2018
Intermittent dynamics in complex systems driven to depletionJuan V Escobar, Isaac Pérez CastilloAmerican 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 WillsArchives of Neurology|January 1, 1984
Familial startle disease (hyperexplexia). Electrophysiologic studiesO N Markand, B P Garg, D D WeaverJournal of Neurosurgery|May 1, 1982
Differential intracranial pressure in patients with unilateral mass lesionsD D Weaver, H R Winn, J A JaneHuman Genetics|January 1, 1982
Pericentric X inversion in dizygotic twins who differ in X chromosome inactivation and menstrual cycle functionE A Keitges, C G Palmer, D D WeaverClinical Genetics|November 1, 1982
Prader-Willi syndrome: are there population differences?M G Butler, D D Weaver, F J MeaneyPageof 12