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Clinical Genetics|October 1, 1980
The use of sequential silver and quinacrine staining to determine the parental origin and breakpoints of a ring-22 human chromosomeG Fowler, B Kaiser-McCaw, F HechtAmerican Journal of Medical Genetics|January 1, 1981
Amniocyte clones for prenatal cytogeneticsF Hecht, D C Peakman, B Kaiser-McCaw, et al.The Western Journal of Medicine|October 1, 1982
Fragile X-linked mental retardation of macro-orchidismB C Moore, T W Glover, B Kaiser-McCaw, et al.International Journal of Cancer|April 15, 1977
Chromosome 14 translocation in African and North American Burkitt's lymphoma;B Kaiser-McCaw, A L Epstein, H S Kaplan, et al.Cancer Genetics and Cytogenetics|October 1, 1983
Acute myeloblastic leukemia (AML) with t(6;9) (p23;q34): a specific subgroup of AML?A A Sandberg, R Morgan, J A McCallister, et al.Cancer Genetics and Cytogenetics|August 1, 1983
Complex cytogenetic findings in acute leukemiaR Morgan, A A Sandberg, B Kaiser-McCaw, et al.Cancer Genetics and Cytogenetics|November 1, 1981
Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemiaF P Li, F Hecht, B Kaiser-McCaw, et al.Blood|June 1, 1978
Clonal evolution in atypical chronic granulocytic leukemia: a non-Philadelphia translocationG C Bagby, B Kaiser-McCaw, F Hecht, et al.Hematological Oncology|January 1, 1984
Bone marrow monosomy 7: hematologic and clinical manifestations in childhood and adolescenceJ J Hutter, F Hecht, B Kaiser-McCaw, et al.Cancer Genetics and Cytogenetics|March 1, 1983
Adenocarcinoma of the gallbladder: chromosome abnormalities in a genetic form of cancerF Hecht, D J Kuban, C Berger, et al.Pageof 14