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Cancer Genetics and Cytogenetics|November 1, 1993
The application of fluorescent in situ hybridization to detect Mbcr/abl fusion in variant Ph chromosomes in CML and ALLG W Dewald, C R Schad, E R Christensen, et al.Cancer Genetics and Cytogenetics|July 1, 1993
Frequency and photographs of HGM11 chromosome anomalies in bone marrow samples from 3,996 patients with malignant hematologic neoplasmsG W Dewald, C R Schad, V C Lilla, et al.Clinical Genetics|March 1, 1996
Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicismN M Lindor, E M Devries, V V Michels, et al.Mayo Clinic Proceedings|November 1, 1994
Efficacy of fluorescence in situ hybridization for detecting PML/RARA gene fusion in treated and untreated acute promyelocytic leukemiaC R Schad, C A Hanson, E Paietta, et al.Clinical Genetics|October 1, 1993
Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16N M Lindor, S M Jalal, S N Thibodeau, et al.Cancer Genetics and Cytogenetics|July 2, 1998
Search for chromosome instability in lymphocytes with germ-line mutations in DNA mismatch repair genesN M Lindor, S M Jalal, T J VanDeWalker, et al.Clinical Chemistry|October 1, 1987
Use of restriction fragment length polymorphism analysis for detecting carriers of "fragile X" syndromeS N ThibodeauAmerican Journal of Medical Genetics|December 11, 1996
Application of fluorescent in situ hybridization with X and Y chromosome specific probes to buccal smear analysisC R Schad, D G Kuffel, W A Wyatt, et al.American Journal of Clinical Pathology|August 1, 1991
Use of fluorescent in situ hybridization for marker chromosome identification in congenital and neoplastic disordersC R Schad, W J Kraker, S M Jalal, et al.Mayo Clinic Proceedings|April 1, 1996
A polymerase chain reaction-based test for spinal and bulbar muscular atrophyZ Wang, S N ThibodeauPageof 20