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American Journal of Medical Genetics|April 1, 1987
Increased sister chromatid exchange frequency at Xq27 site in affected fragile X malesS L Wenger, J C Hennessey, M W SteeleClinical Genetics|February 1, 1984
In vitro reversal of fragile-X expression by exogenous thymidineG B Gardiner, S L Wenger, M W SteeleAmerican Journal of Medical Genetics|April 1, 1990
Mosaicism in Pallister i(12p) syndromeS L Wenger, L Y Boone, M W SteeleAnnales De Genetique|January 1, 1991
Assessment of X bends in patients with atypical X chromosome phenotypesC A Munn, S L Wenger, M W SteeleClinical Genetics|September 1, 1988
Risk effect of maternal age in Pallister i(12p) syndromeS L Wenger, M W Steele, W D YuJournal of Medical Genetics|April 1, 1988
Clinical consequences of deletion 1p35S L Wenger, M W Steele, D J BeckerHuman Genetics|October 1, 1990
X chromosome imprinting in fragile X syndromeW D Yu, S L Wenger, M W SteeleIn Vitro|August 1, 1981
Incorporation of bacteriophage DNA into the genome of cultured human lymphocytesS L Wenger, M W Steele, J H TurnerJAMA|January 9, 1978
Prostaglandin synthetase inhibitors in Bartter's syndrome. Effect on immunoreactive prostaglandin E excretionR E Bowden, J R Gill, N Radfar, et al.Clinical Genetics|February 1, 1983
A simplified PKU gene carrier detection test using fasting bloodB Tenenholz, S L Wenger, J Breck, et al.Pageof 66