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American Journal of Human Genetics|July 1, 1989
Hypopigmentation: a common feature of Prader-Labhart-Willi syndromeM G ButlerAmerican Journal of Medical Genetics|March 1, 1990
Prader-Willi syndrome: current understanding of cause and diagnosisM G ButlerClinical Dysmorphology|January 29, 2000
A 68-year-old white female with Prader-Willi syndromeM G ButlerJournal of Intellectual Disability Research : JIDR|April 8, 2017
Clinical and genetic aspects of the 15q11.2 BP1-BP2 microdeletion disorderM G ButlerAmerican Journal of Medical Genetics|December 8, 1998
Methylation PCR analysis of Prader-Willi syndrome, Angelman syndrome, and control subjectsB Muralidhar, M G ButlerClinical Genetics|November 1, 1994
Antley-Bixler syndrome: report of a patient and review of literatureS Hassell, M G ButlerClinical Genetics|April 1, 1984
Dermatoglyphic features in Prader-Willi syndrome with respect to chromosomal findingsT Reed, M G ButlerClinical Genetics|February 5, 2005
Insulin resistance and obesity-related factors in Prader-Willi syndrome: comparison with obese subjectsZ Talebizadeh, M G ButlerSouthern Medical Journal|March 1, 1995
Blood specimens from patients referred for cytogenetic analysis: Vanderbilt University experience from 1985 to 1992M G Butler, T HamillMechanisms 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 LanePageof 18