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Journal of Human Genetics|February 24, 2001
The BRCA2 genetic variant IVS7 + 2T-->G is a mutationM T Pyne, A R Brothman, B Ward, et al.Journal of Medical Genetics|May 15, 2003
Application of haplotype pair analysis for the identification of hemizygous lociB C Hendrickson, D Pruss, E Lyon, et al.Mutation Research|September 10, 1999
A characterization of genetic variants in BRCA1 intron 8 identifies a mutation and a polymorphismM T Pyne, D Pruss, B E Ward, et al.American Journal of Medical Genetics|July 16, 1999
BRCA1 IVS16+6T-->C is a deleterious mutation that creates an aberrant transcript by activating a cryptic splice donor siteT Scholl, M T Pyne, D Russo, et al.Cancer Genetics and Cytogenetics|May 1, 1997
Cytogenetic studies in prostate cancer: are we making progress?A R BrothmanCytogenetics and Cell Genetics|January 1, 1992
Characterization of 10 marker chromosomes in a prostatic cancer cell line by in situ hybridizationA R Brothman, A M PatelExperimental Cell Research|March 1, 1984
Actinomycin D in low concentrations binds uniformly to human chromosomesA R Brothman, T J LindellCytogenetic and Genome Research|September 22, 2011
Clinical laboratory implementation of cytogenomic microarraysS T South, A R BrothmanAmerican Journal of Medical Genetics|March 15, 1993
Multiple craniofacial anomalies associated with an interstitial deletion of chromosome 1(q21->q25)L G Leichtman, D Strum, A R BrothmanAmerican Journal of Medical Genetics|September 20, 2002
Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4A Battaglia, A R Brothman, J C CareyPageof 169