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Clinical Genetics|November 4, 2004
DHCR7 mutations and genotype-phenotype correlation in 37 Polish patients with Smith-Lemli-Opitz syndromeE Ciara, M J M Nowaczyk, M Witsch-Baumgartner, et al.
The Journal of Biological Chemistry|August 25, 1984
Abnormal lecithin:cholesterol acyltransferase activation by a human apolipoprotein A-I variant in which a single lysine residue is deletedS C Rall, K H Weisgraber, R W Mahley, et al.
Analytical and Bioanalytical Chemistry|September 12, 2006
Single-detector micro-electro-mechanical scanning grating spectrometerM Kraft, A Kenda, A Frank, et al.
Metabolism: Clinical and Experimental|July 1, 1996
Effects of pancreas transplantation on distribution and composition of plasma lipoproteinsB Föger, A Königsrainer, G Palos, et al.
Waste Management & Research : the Journal of the International Solid Wastes and Public Cleansing Association, ISWA|July 12, 2014
By-products from the biodiesel chain as a substrate to citric acid production by solid-state fermentationManuella Schneider, Gabriela F Zimmer, Ezequiel B Cremonese, et al.
Cytogenetic and Genome Research|April 21, 2012
Parental origin of de novo cytogenetically balanced reciprocal non-Robertsonian translocationsM Höckner, A Spreiz, A Frühmesser, et al.
Annals of Hematology|June 1, 1996
Interferon alpha-2c therapy of patients with chronic myelogenous leukemia: long-term results of a multicenter phase-II study. Austrian Biological Response Modifier (BRM) Study GroupJ Thaler, G Gastl, T Fluckinger, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 25, 2000
Lipoprotein(a) determination and risk of cardiovascular disease in South African patients with familial hypercholesterolaemiaC L Scholtz, A Lingenhel, R Hillermann, et al.
Gene|May 16, 1998
Characterization of the human gene coding for the swelling-dependent chloride channel ICln at position 11q13.5-14.1 (CLNS1A) and further characterization of the chromosome 6 (CLNS1B) localizationU O Nagl, M Erdel, F Bergmann, et al.
The Journal of Clinical Investigation|October 1, 1981
Familial dysbetalipoproteinemia. Abnormal binding of mutant apoprotein E to low density lipoprotein receptors of human fibroblasts and membranes from liver and adrenal of rats, rabbits, and cowsW J Schneider, P T Kovanen, M S Brown, et al.
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