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Cancer Genetics and Cytogenetics|March 1, 1985
A complex translocation in acute promyelocytic leukemiaD F Callen, B M Dale, R E Sage, et al.Science (New York, N.Y.)|December 8, 1989
A new DNA marker tightly linked to the fragile X locus (FRAXA)G K Suthers, D F Callen, V J Hyland, et al.American Journal of Medical Genetics|July 1, 1992
Molecular cytogenetic and clinical studies of 42 patients with marker chromosomesD F Callen, H Eyre, M Y Yip, et al.Biochemical and Biophysical Research Communications|February 13, 2001
Isolation, tissue distribution, and chromosomal localization of a novel testis-specific human four-transmembrane gene related to CD20 and FcepsilonRI-betaM D Hulett, E Pagler, J R Hornby, et al.American Journal of Surgery|May 1, 1982
Abdominal lymphoma: lack of complete surgical stagingS Ondreyco, H J Eyre, C Kjeldsberg, et al.Cell|February 7, 1997
Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeatS Yu, M Mangelsdorf, D Hewett, et al.Clinical Genetics|November 1, 1992
De novo interstitial deletion 16(q12.1q13) of paternal origin in a 10-year-old boyS Schuffenhauer, D F Callen, H Seidel, et al.Genomics|September 1, 1994
Thermolabile phenol sulfotransferase gene (STM): localization to human chromosome 16p11.2I A Aksoy, D F Callen, S Apostolou, et al.Genomics|August 1, 1991
Human chromosome 16 physical map: mapping of somatic cell hybrids using multiplex PCR deletion analysis of sequence tagged sitesR I Richards, K Holman, S Lane, et al.Medical and Pediatric Oncology|January 1, 1975
Study of leukocyte kinetics in acute myelocytic leukemia utilizing chromium-51P J Rosen, H J Eyre, D L Lilien, et al.Pageof 264