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Retina (Philadelphia, Pa.)|January 1, 1985
The retinopathy of primary hyperoxaluriaE I Traboulsi, F el-Baba, A Y Barakat, et al.Mechanisms of Ageing and Development|January 1, 1989
Effects of age, sex and multiple endocrine neoplasia type-II on silver stained nucleolar organizer regionsM G Butler, J R LaneDiagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|December 1, 1995
Use of fluorescence in situ hybridization (FISH) in the diagnosis of DiGeorge sequence and related diseasesR S Larson, M G ButlerAmerican Journal of Medical Genetics|December 1, 1988
Do some patients with fragile X syndrome have precocious puberty?M G Butler, J L NajjarAmerican Journal of Physical Anthropology|December 1, 1987
Craniofacial variation and growth in the Prader-Labhart-Willi syndromeF J Meaney, M G ButlerJournal of Clinical Epigenetics|January 24, 2017
Examination of Global Methylation and Targeted Imprinted Genes in Prader-Willi SyndromeA M Manzardo, M G ButlerAmerican Journal of Medical Genetics|February 1, 1987
An anthropometric study of 38 individuals with Prader-Labhart-Willi syndromeM G Butler, F J MeaneyPediatrics|October 1, 1991
Standards for selected anthropometric measurements in Prader-Willi syndromeM G Butler, F J MeaneyJournal of Intellectual Disability Research : JIDR|April 1, 1993
Clinical and cytogenetic survey of institutionalized mentally retarded patients with emphasis on the fragile-X syndromeM G Butler, D N SinghAmerican Journal of Medical Genetics|December 1, 1987
Sister chromatid exchange analysis in the Prader-Labhart-Willi syndromeM G Butler, B B JenkinsPageof 18