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European Journal of Human Genetics : EJHG|February 28, 2008
Associations of apolipoprotein E gene with ischemic stroke and intracranial atherosclerosisShérine Abboud, Leena E Viiri, Dieter Lütjohann, et al.
European Journal of Human Genetics : EJHG|February 28, 2008
No association between MUTYH and MSH6 germline mutations in 64 HNPCC patientsVerena Steinke, Nils Rahner, Monika Morak, et al.
European Journal of Human Genetics : EJHG|March 7, 2008
Genome-wide search for QTLs for apolipoprotein A-I level in elderly Swedish DZ twins: evidence of female-specific locus on 15q11-13Patrik K E Magnusson, Marcus Boman, Ulf de Faire, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Universal screening for hemoglobinopathies using high-performance liquid chromatography: clinical results of 2.2 million screensF Lorey, G Cunningham, F Shafer, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Mapping of Friedreich's ataxia locus by identification of recombination events in patients homozygous by descentE Monrós, P Smeyers, F Rodius, et al.
European Journal of Human Genetics : EJHG|July 20, 2007
Branchio-oto-renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analysesKirsten Marie Sanggaard, Nanna Dahl Rendtorff, Klaus Wilbrandt Kjaer, et al.
European Journal of Human Genetics : EJHG|July 20, 2007
Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf-Hirschhorn syndromeKlara Flipsen-ten Berg, Peter M van Hasselt, Marc J Eleveld, et al.
European Journal of Human Genetics : EJHG|August 31, 2006
Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriersMarzena Gajecka, Caron D Glotzbach, Malgorzata Jarmuz, et al.
European Journal of Human Genetics : EJHG|October 19, 2006
Implication of abnormal epigenetic patterns for human diseasesC B Santos-Rebouças, M M G Pimentel
European Journal of Human Genetics : EJHG|October 7, 2006
Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisationChristian H Brenk, Eva-Christina Prott, Detlef Trost, et al.
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