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Human Genetics|February 1, 1992
Mutational analysis of SRY: nonsense and missense mutations in XY sex reversalJ R Hawkins, A Taylor, P Berta, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Characterization and mapping of the human SOX4 geneC J Farr, D J Easty, J Ragoussis, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Isolation of new probes from Xq12-->q13: an example of the screening of reference libraries with Alu-PCR products from radiation hybridsF Muscatelli, A P Monaco, P N Goodfellow, et al.
The EMBO Journal|December 1, 1992
SRY, like HMG1, recognizes sharp angles in DNAS Ferrari, V R Harley, A Pontiggia, et al.
Human Genetics|May 1, 1988
Characterization of a partial deletion of the factor VIII gene in a haemophiliac with inhibitorB Bardoni, M Sampietro, M Romano, et al.
Genetic Epidemiology|January 1, 1997
Empirical genomewide significance levels established by whole genome simulationsS Sawcer, H B Jones, D Judge, et al.
Science (New York, N.Y.)|December 16, 1988
Human T cell leukemia viruses use a receptor determined by human chromosome 17M A Sommerfelt, B P Williams, P R Clapham, et al.
Journal of Endocrinological Investigation|March 24, 2006
X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism: report on new mutation of the DAX-1 gene in two siblingsV Calvari, M G Alpigiani, E Poggi, et al.
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