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Journal of Medical Genetics|March 1, 1995
Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndromeJ N Macpherson, G Curtis, J A Crolla, et al.Human Genetics|July 8, 1998
A study of females with deletions of the short arm of the X chromosomeR S James, B Coppin, P Dalton, et al.European Journal of Clinical Investigation|October 1, 1989
The effect of testosterone replacement on plasma lipids and apolipoproteinsD B Jones, B Higgins, J S Billet, et al.Nature|May 17, 1984
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28S S Bhattacharya, A F Wright, J F Clayton, et al.American Journal of Human Genetics|September 1, 1991
Trisomy 21: association between reduced recombination and nondisjunctionS L Sherman, N Takaesu, S B Freeman, et al.Chemical Communications (Cambridge, England)|January 29, 2010
Molecular sieve properties of mesoporous silica with intraporous nanocarbonF de Clippel, A Harkiolakis, X Ke, et al.American Journal of Human Genetics|April 1, 1995
Cytogenetic and molecular studies of Down syndrome individuals with leukemiaJ J Shen, B J Williams, A Zipursky, et al.Proceedings of the National Academy of Sciences of the United States of America|February 1, 1986
Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markersI Oberlé, R Heilig, J P Moisan, et al.Cell|February 22, 1991
Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndromeM V Bell, M C Hirst, Y Nakahori, et al.Nature|June 12, 1997
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive functionD H Skuse, R S James, D V Bishop, et al.Pageof 17