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Nature Genetics|November 5, 1997
Male-driven evolution of DNA sequences in birdsH Ellegren, A K FridolfssonNature Genetics|November 5, 1997
Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosaM A Maw, B Kennedy, A Knight, et al.Nature Genetics|November 5, 1997
Drosophila CBP is required for dorsal-dependent twist gene expressionH Akimaru, D X Hou, S IshiiNature Genetics|November 5, 1997
Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndromeL Pereira, K Andrikopoulos, J Tian, et al.Nature Genetics|November 5, 1997
Human telomeres contain two distinct Myb-related proteins, TRF1 and TRF2D Broccoli, A Smogorzewska, L Chong, et al.Nature Genetics|May 20, 1998
Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndromeS D Dreyer, G Zhou, A Baldini, et al.Nature Genetics|May 20, 1998
Homozygous C1q deficiency causes glomerulonephritis associated with multiple apoptotic bodiesM Botto, C Dell'Agnola, A E Bygrave, et al.Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.Nature Genetics|May 20, 1998
SMN oligomerization defect correlates with spinal muscular atrophy severityC L Lorson, J Strasswimmer, J M Yao, et al.Pageof 742