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Human Genetics|January 1, 1985
Human chromosome variation with two Robertsonian translocationsR Morgan, H Bixenman, F HechtClinical Genetics|February 1, 1986
Congenital cutis laxa with retardation of growth and motor development: a recessive disorder of connective tissue with male lethalityJ Allanson, W Austin, F HechtClinical 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'KeeffeInternational Journal of Paediatric Dentistry|April 20, 2001
Dental caries in schoolchildren of an Estonian and a Danish municipalityE Dragheim, P E Petersen, I Kalo, et al.Pageof 16