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European Journal of Human Genetics : EJHG|January 20, 2005
Linkage disequilibrium patterns vary substantially among populationsSarah L Sawyer, Namita Mukherjee, Andrew J Pakstis, et al.
European Journal of Human Genetics : EJHG|January 20, 2005
Polymorphisms in APOA1 and LPL genes are statistically independently associated with fasting TG in men with CADOlga W Souverein, J Wouter Jukema, S Matthijs Boekholdt, et al.
European Journal of Human Genetics : EJHG|January 20, 2005
Patients with familial biparental hydatidiform moles have normal methylation at imprinted genesOsman El-Maarri, Muhieddine Seoud, Jean-Baptiste Rivière, et al.
European Journal of Human Genetics : EJHG|January 14, 2022
Polygenic risk modeling for prediction of epithelial ovarian cancer riskEileen O Dareng, Jonathan P Tyrer, Daniel R Barnes, et al.
European Journal of Human Genetics : EJHG|January 15, 2022
Where is genetic medicine headed? Exploring the perspectives of Canadian genetic professionals on future trends using the Delphi methodKennedy Borle, Nicola Kopac, Nick Dragojlovic, et al.
European Journal of Human Genetics : EJHG|January 16, 2022
Bi-allelic SMO variants in hypothalamic hamartoma: a recessive cause of Pallister-Hall syndromeTimothy E Green, Mareike Schimmel, Susanna Schubert, et al.
European Journal of Human Genetics : EJHG|November 27, 2021
Genomic analysis of childhood hearing loss in the Yoruba population of NigeriaAdebolajo Adeyemo, Rabia Faridi, Parna Chattaraj, et al.
European Journal of Human Genetics : EJHG|November 24, 2021
A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trialLieke M van den Heuvel, Yvonne M Hoedemaekers, Annette F Baas, et al.
European Journal of Human Genetics : EJHG|November 2, 2022
Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformationsJulia Fabian, Gabriel C Dworschak, Lea Waffenschmidt, et al.
European Journal of Human Genetics : EJHG|April 7, 2019
Linkage analysis revealed risk loci on 6p21 and 18p11.2-q11.2 in familial colon and rectal cancer, respectivelySusanna von Holst, Xiang Jiao, Wen Liu, et al.
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