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Genomics|May 1, 1992
Somatic cell hybrid deletion map of human chromosome 18A D Kline, K Rojas, R Mewar, et al.American Journal of Medical Genetics|September 14, 1999
Characterization of a complex chromosomal rearrangement in a patient with a typical catlike cry and no other clinical findings of cri-du-chat syndromeC Sreekantaiah, D Kronn, R C Marinescu, et al.Annals of Human Genetics|May 1, 1991
The molecular basis and diagnosis of familial hypercholesterolaemia in South African AfrikanersM J Kotze, E Langenhoven, L Warnich, et al.Journal of Medical Genetics|May 1, 1990
An exon 4 mutation identified in the majority of South African familial hypercholesterolaemicsM J Kotze, L Warnich, E Langenhoven, et al.Journal of Medical Genetics|June 1, 1991
Deletion of chromosome 13 in Moebius syndromeJ J Slee, R D Smart, D L ViljoenCancer|December 1, 1979
Chromosome changes in 17 human neoplasms studied with bandingM F van der Riet-Fox, A E Retief, W A van NiekerkSouth African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|October 21, 1989
Molecular characterisation of a low-frequency mutation in exon 8 of the human low-density lipoprotein receptor geneM J Kotze, E Langenhoven, L Warnich, et al.South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|April 18, 1981
Ultrasound examination before amniocentesis. Its effect on cell culture for cytogenetic studiesR D Smart, M M Nelson, E J CoetzeeGenomics|January 1, 1995
The structural genes, MEP1A and MEP1B, for the alpha and beta subunits of the metalloendopeptidase meprin map to human chromosomes 6p and 18q, respectivelyJ S Bond, K Rojas, J Overhauser, et al.American Journal of Human Genetics|June 1, 1994
Interstitial deletions are not the main mechanism leading to 18q deletionsG Strathdee, W Harrison, H C Riethman, et al.Pageof 13