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Human Genetics|July 1, 1996
A molecular anatomical analysis of mosaic trisomy 16J M Greally, K Neiswanger, J H Cummins, et al.Human Genetics|May 13, 2015
Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-upFan Liu, Mijke Visser, David L Duffy, et al.Human Genetics|May 20, 2015
Telomere length and common disease: study design and analytical challengesJennifer H Barrett, Mark M Iles, Alison M Dunning, et al.Human Genetics|November 6, 2010
Mutation analysis in Bardet-Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individualsSabine Janssen, Gokul Ramaswami, Erica E Davis, et al.Human Genetics|August 1, 1990
HLA class I gene polymorphism in genetic hemochromatosisA M Jouanolle, J Yaouanq, M Blayau, et al.Human Genetics|August 1, 1990
Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophyK V Walsh, H G Harley, J D Brook, et al.Human Genetics|September 18, 2009
Detection and characterisation of large SERPINC1 deletions in type I inherited antithrombin deficiencyVéronique Picard, Jian-Min Chen, Brigitte Tardy, et al.Human Genetics|September 18, 2009
Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetesJanniche Torsvik, Stefan Johansson, Anders Johansen, et al.Human Genetics|February 23, 2011
Recent progress in the study of the genetics of heightGuillaume LettreHuman Genetics|February 1, 2011
Genetic analysis of biological pathway data through genomic randomizationBrian L Yaspan, William S Bush, Eric S Torstenson, et al.Pageof 959