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Human Genetics|September 1, 1995
Two highly polymorphic CA repeats in the Menkes gene (ATP7A)C R Begy, H A Dierick, J W Innis, et al.Proceedings of the National Academy of Sciences of the United States of America|June 1, 1987
Microcell-mediated transfer of a single human chromosome complements xeroderma pigmentosum group A fibroblastsR A Schultz, P J Saxon, T W Glover, et al.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 HechtCancer Genetics and Cytogenetics|October 1, 1988
Robertsonian chromosome recombinants are rare in cancerF Hecht, R Morgan, B K HechtThe New England Journal of Medicine|January 9, 1975
Parthenogenic origin of benign ovarian teratomasD Linder, B K McCaw, F HechtAmerican Journal of Medical Genetics|August 1, 1989
Three additional cases of the congenital hypothalamic "hamartoblastoma" (Pallister-Hall) syndromeP D Pallister, F Hecht, J HerrmanAmerican Journal of Medical Genetics|June 1, 1985
Enhanced expression of chromosome fragile site 10q25 in chronic myelogenous leukemiaR Morgan, S S Morgan, F HechtInternational Journal of Radiation Oncology, Biology, Physics|February 1, 1985
Unexpected lambda chain expression in lymphocytic malignancyF Hecht, R Morgan, B K HechtPrenatal Diagnosis|July 1, 1982
Sacrococcygeal teratoma: prenatal diagnosis with elevated alphafetoprotein and acetylcholinesterase in amniotic fluidF Hecht, B K Hecht, D O'KeeffeAmerican Journal of Medical Genetics|March 1, 1989
Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37)J L Gorski, B A Cox, M Kyine, et al.Pageof 22