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Journal of Intellectual Disability Research : JIDR|April 8, 2017
Clinical and genetic aspects of the 15q11.2 BP1-BP2 microdeletion disorderM G ButlerThe International Journal of Pediatric Nephrology|April 1, 1986
Hypokalemic alkalosis, hyperreninemia, aldosteronism, normal blood pressure and normal juxtaglomerular apparatus--a new syndrome of renal alkalosisA Y Barakat, Y K Francis, A A MufarrijLe Journal Medical Libanais. the Lebanese Medical Journal|January 1, 1989
The incidence of congenital abnormalities of the kidney and urogenital system in LebanonA Y Barakat, G M Baasiri, N A MounlaAmerican 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 HamillMetabolic, Pediatric, and Systemic Ophthalmology (New York, N.Y. : 1985)|January 1, 1985
Ocular abnormalities and renal disease: a reviewA Y Barakat, S I Butrus, B M Faris, et al.The Journal of Pediatrics|July 1, 1977
Familial nephrosis, nerve deafness, and hypoparathyroidismA Y Barakat, J B D'Albora, M M Martin, et al.Pageof 18