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South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|February 19, 1977
Antenatal diagnosis of Hurler's syndromeH E Henderson, M M NelsonAmerican Journal of Medical Genetics. Supplement|January 1, 1986
An association of caudal malformations arising from a defect in the "axial mesoderm" developmental fieldR J Gardner, M M NelsonBritish Medical Journal|March 6, 1971
Associations between drugs administered during pregnancy and congenital abnormalities of the fetusM M Nelson, J O ForfarMolecular Biology & Medicine|December 1, 1990
Frameshift mutation in exon 3 of the lipoprotein lipase gene causes a premature stop codon and lipoprotein lipase deficiencyH E Henderson, R Devlin, J Peterson, et al.American Journal of Human Genetics|September 1, 1986
Subregional assignment of the linked marker G8 (D4S10) for Huntington disease to chromosome 4p16.1-16.3H S Wang, C R Greenberg, J Hewitt, et al.Genomics|June 1, 1992
Nonrandom association between Huntington disease and two loci separated by about 3 Mb on 4p16.3S Andrew, J Theilmann, A Hedrick, et al.Proceedings of the National Academy of Sciences of the United States of America|February 1, 1989
A major insertion accounts for a significant proportion of mutations underlying human lipoprotein lipase deficiencyS Langlois, S Deeb, J D Brunzell, et al.The Pharmacogenomics Journal|October 26, 2016
The global spectrum of protein-coding pharmacogenomic diversityG E B Wright, B Carleton, M R Hayden, et al.Clinical Genetics|October 31, 2001
The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery diseaseS M Clee, O Loubser, J Collins, et al.Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1996
Origin and migration of an Afrikaner founder mutation FHAfrikaner-2 (V408M) causing familial hypercholesterolemiaJ C Defesche, D E Van Diermen, M R Hayden, et al.Pageof 34