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American Journal of Medical Genetics|July 1, 1991
Creativity in medical genetics and dysmorphologyF Hecht, B K 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 HechtBlood|February 1, 1988
Clinical and biologic characterization of T-cell neoplasias with rearrangements of chromosome 7 band q34S D Smith, R Morgan, R Gemmell, 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 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 HerrmanPrenatal Diagnosis|July 1, 1982
Sacrococcygeal teratoma: prenatal diagnosis with elevated alphafetoprotein and acetylcholinesterase in amniotic fluidF Hecht, B K Hecht, D O'KeeffeHuman Genetics|August 1, 1990
Chromosomes 17 and 22 involved in marker formation in neurofibrosarcoma in von Recklinghausen disease. A cytogenetic and in situ hybridization studyH J Decker, L A Cannizzaro, M J Mendez, et al.Cancer Genetics and Cytogenetics|May 1, 1987
Fragile sites limited to lymphocytes: molecular recombination and malignancyF Hecht, B K Hecht, I R KirschCancer Genetics and Cytogenetics|January 1, 1990
A guide to fragile sites on human chromosomesF Hecht, K H Ramesh, D H LockwoodPageof 202