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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.
The New England Journal of Medicine|July 8, 1982
Myelomatosis with type III hyperlipoproteinemia: clinical and metabolic studiesC Cortese, B Lewis, N E Miller, et al.
American Journal of Human Genetics|March 26, 1999
mtDNA analysis of Nile River Valley populations: A genetic corridor or a barrier to migration?M Krings, A E Salem, K Bauer, et al.
Clinical Genetics|June 30, 2010
Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysisV Grossmann, M Höckner, H Karmous-Benailly, et al.
Clinical Genetics|October 15, 2013
Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomaliesA Spreiz, E Haberlandt, M Baumann, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndromeA Silahtaroglu, F A Hol, P K Jensen, et al.
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