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Genes, Chromosomes & Cancer|January 1, 1991
Molecular and cytogenetic analysis of tumors in von Recklinghausen neurofibromatosisT W Glover, C K Stein, E Legius, et al.American Journal of Mental Retardation : AJMR|January 1, 1993
Conversational roles of children with developmental delays and their mothers in natural and semi-structured situationsB F Hecht, H G Levine, A B MastergeorgeHuman Genetics|October 1, 1989
Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosisD H Lockwood, A Farrier, F Hecht, et al.Environmental Health Perspectives|August 1, 1979
New translocations in human lymphocytes: a mutagen monitoring systemF Hecht, B K McCaw, D Peakman, et al.Genes, Chromosomes & Cancer|October 27, 1999
Germline mutations in NF1 patients with malignanciesR Wu, C López-Correa, J L Rutkowski, et al.American Journal of Human Genetics|June 1, 1991
Localization of the translocation breakpoint in a female with Menkes syndrome to Xq13.2-q13.3 proximal to PGK-1V Verga, B K Hall, S R Wang, et al.Human Molecular Genetics|February 1, 1996
FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sitesC M Wilke, B K Hall, A Hoge, et al.Cancer Genetics and Cytogenetics|March 1, 1988
Fragile sites at 4q23 and 7q11.23 unique to bone marrow cellsR Morgan, S S Morgan, B K Hecht, et al.Cancer Genetics and Cytogenetics|November 1, 1985
Translocation (1;7)(p11;p11): a new myeloproliferative hematologic entityA A Sandberg, R Morgan, B K Hecht, et al.JAMA|December 8, 1998
Postexposure prophylaxis after nonoccupational HIV exposure: clinical, ethical, and policy considerationsP Lurie, S Miller, F Hecht, et al.Pageof 22