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Annals of Human Genetics|July 23, 2011
Association of COL1A1 and TGFB1 polymorphisms with otosclerosis in a Tunisian populationAyda Khalfallah, Isabelle Schrauwen, Malek Mnejja, et al.Annals of Human Genetics|June 15, 2007
Leukocyte cDNA analysis of NSD1 derived from confirmed Sotos syndrome patientsM Duno, F Skovby, M SchwartzAnnals of Human Genetics|June 21, 2007
A novel approach to detect parent-of-origin effects from pedigree data with application to Beckwith-Wiedemann syndromeSanjay Shete, Robert C Elston, Yue LuAnnals of Human Genetics|June 26, 2007
Fine mapping of disease genes using tagging SNPsArvid Sjölander, Ola Hössjer, Linda Werner Hartman, et al.Annals of Human Genetics|March 13, 2012
Genetic variant R952Q in LRP8 is associated with increased plasma triglyceride levels in patients with early-onset CAD and MIGong-Qing Shen, Lin Li, Qing K WangAnnals of Human Genetics|December 20, 2011
Meta analysis of the association between MTHFR C677T polymorphism and the risk of congenital heart defectsMeng Yin, Lingyan Dong, Jinghao Zheng, et al.Annals of Human Genetics|July 1, 1990
Assignment of the human nicotinic acetylcholine receptor genes: the alpha and delta subunit genes to chromosome 2 and the beta subunit gene to chromosome 17D Beeson, S Jeremiah, L F West, et al.Annals of Human Genetics|July 1, 1990
A cytogenetic and molecular reappraisal of a series of patients with Turner's syndromeP A Jacobs, P R Betts, A E Cockwell, et al.Annals of Human Genetics|August 13, 2011
A mutation in cartilage oligomeric matrix protein (COMP) causes early-onset osteoarthritis in a large kindred studyShu-Chi Mu, Yi-Jung Lin, Hwa-Chang Liu, et al.Annals of Human Genetics|October 25, 2011
mtDNA lineages reveal coronary artery disease-associated structures in the Lebanese populationMarc Haber, Sonia C Youhanna, Oleg Balanovsky, et al.Pageof 231