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Genomics|July 15, 1996
cDNA cloning, tissue distribution, and chromosomal localization of myelodysplasia/myeloid leukemia factor 2 (MLF2)M U Kuefer, A T Look, D C Williams, et al.Genes & Development|May 27, 1999
Apc1638T: a mouse model delineating critical domains of the adenomatous polyposis coli protein involved in tumorigenesis and developmentR Smits, M F Kielman, C Breukel, et al.Cancer Research|March 8, 2000
The DNA mismatch repair genes Msh3 and Msh6 cooperate in intestinal tumor suppressionW Edelmann, A Umar, K Yang, et al.American Journal of Human Genetics|October 27, 1997
Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patientsC Carlson, H Sirotkin, R Pandita, et al.Genomics|November 5, 1997
A sequence-ready physical map of a region of 12q24.1B Renault, A Hovnanian, S Bryce, et al.Nature Genetics|December 30, 1999
Cardiac defects and renal failure in mice with targeted mutations in Pkd2G Wu, G S Markowitz, L Li, et al.Nature Genetics|January 1, 1997
Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndromeC T Basson, D R Bachinsky, R C Lin, et al.Journal of the American Medical Informatics Association : JAMIA|November 1, 1995
Internet-based support for bioscience research: a collaborative genome center for human chromosome 12P L Miller, P M Nadkarni, K K Kidd, et al.Genomics|October 1, 1996
Linkage of asthma and total serum IgE concentration to markers on chromosome 12q: evidence from Afro-Caribbean and Caucasian populationsK C Barnes, J D Neely, D L Duffy, et al.Nature Genetics|March 18, 1999
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier diseaseA Sakuntabhai, V Ruiz-Perez, S Carter, et al.Pageof 12