Showing results (181-190 of 324) with videos related to
Sort By:
Pageof 33
Human Molecular Genetics|February 1, 1997
A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3S S Chong, S D Pack, A V Roschke, et al.Journal of Medical Genetics|January 3, 2001
Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14P Ungaro, S L Christian, J A Fantes, et al.American Journal of Human Genetics|July 1, 1995
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patientsS L Christian, W P Robinson, B Huang, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 1, 1992
Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q13-14M Labuda, T M Fujiwara, M V Ross, et al.Human Genetics|April 1, 1992
Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia using the polymerase chain reactionD Owerbach, M B Draznin, R J Carpenter, et al.Human Molecular Genetics|February 1, 1994
Olfactory receptor gene cluster on human chromosome 17: possible duplication of an ancestral receptor repertoireN Ben-Arie, D Lancet, C Taylor, et al.Genes, Chromosomes & Cancer|July 1, 1990
Cloning and characterization of the t(15;17) translocation breakpoint region in acute promyelocytic leukemiaR S Lemons, D Eilender, R A Waldmann, et al.Clinical Genetics|August 1, 1992
X-linked lymphoproliferative disease: prenatal detection of an unaffected histocompatible maleJ C Mulley, A M Turner, A K Gedeon, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1989
Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sourcesD L Nelson, S A Ledbetter, L Corbo, et al.Journal of Craniofacial Genetics and Developmental Biology|April 1, 1996
Unilateral cleft lip in a boy with Angelman syndromeO Rösby, P Strömme, M Sandsmark, et al.Pageof 33