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Pediatric Dermatology|March 27, 2003
Xp22.3 microdeletion in a 19-year-old girl with clinical features of MLS syndromeF Enright, P Campbell, R L Stallings, et al.Genomics|November 1, 1989
Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19L H Thompson, L L Bachinski, R L Stallings, et al.Cytogenetic and Genome Research|June 26, 2004
Evolution of unbalanced gain of distal chromosome 2p in neuroblastomaR L Stallings, P Carty, L McArdle, et al.American Journal of Human Genetics|May 1, 1994
Evidence of linkage disequilibrium in the Spanish polycystic kidney disease I populationB Peral, C J Ward, J L San Millán, et al.Genomics|December 1, 1993
Identification and regional localization of a human IMP dehydrogenase-like locus (IMPDHL1) at 16p13.13N A Doggett, D F Callen, Z L Chen, et al.Cell Death and Differentiation|January 8, 2011
MicroRNAs 10a and 10b are potent inducers of neuroblastoma cell differentiation through targeting of nuclear receptor corepressor 2N H Foley, I Bray, K M Watters, et al.Cytogenetics and Cell Genetics|January 1, 1987
Chromosomal assignment of amplified genes in hydroxyurea-resistant hamster cellsP N Tonin, R L Stallings, M D Carman, et al.Biotechniques|June 1, 1991
A program for computer-assisted scoring of Southern blotsT M Cannon, R J Koskela, C Burks, et al.Chromosoma|January 1, 1985
Oncogenes and linkage groups: conservation during mammalian chromosome evolutionR L Stallings, A C Munk, J L Longmire, et al.Proceedings of the National Academy of Sciences of the United States of America|August 1, 1990
Physical mapping of human chromosomes by repetitive sequence fingerprintingR L Stallings, D C Torney, C E Hildebrand, et al.Pageof 7