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Genomics|November 1, 1992
Genetic heterogeneity in X-linked amelogenesis imperfectaM J Aldred, P J Crawford, E Roberts, et al.Cytogenetic and Genome Research|May 8, 2009
A complex medical phenotype in a patient with triplication of 2q12.3 to 2q13 characterized with oligonucleotide array CGHC L Mercer, C E Browne, J C K Barber, et al.American Journal of Human Genetics|July 10, 2001
Maternal folate polymorphisms and the etiology of human nondisjunctionT J Hassold, L C Burrage, E R Chan, et al.Journal of Immunology (Baltimore, Md. : 1950)|March 24, 1998
The A-Myb transcription factor is a marker of centroblasts in vivoJ Golay, V Broccoli, G Lamorte, et al.Journal of Medical Genetics|December 1, 1994
X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684)N Dahl, F Samson, N S Thomas, 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.Human Molecular Genetics|October 1, 1993
Characterisation of molecular DNA rearrangements within the Xq12-q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA)N S Thomas, J Chelly, J Zonana, et al.The Journal of Biological Chemistry|April 27, 2001
BCR-ABL and interleukin 3 promote haematopoietic cell proliferation and survival through modulation of cyclin D2 and p27Kip1 expressionY Parada, L Banerji, J Glassford, et al.Journal of Medical Genetics|July 1, 1991
Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindredA F Wright, S S Bhattacharya, M A Aldred, et al.Human Genetics|January 1, 1985
Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophyC S Brown, N S Thomas, M Sarfarazi, et al.Pageof 66