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Annals of Human Genetics|May 1, 1991
Assignment of eight human genomic DNA sequences detecting high frequency restriction fragment length polymorphismsN K Spurr, D Kelsell, L Rooke, et al.
Annals of Human Genetics|December 15, 2006
Association of a common interferon regulatory factor 5 (IRF5) variant with increased risk of systemic lupus erythematosus (SLE)F Y K Demirci, S Manzi, R Ramsey-Goldman, et al.
Annals of Human Genetics|June 9, 2006
The role of self-defined race/ethnicity in population structure controlX-Q Liu, A D Paterson, E M John, et al.
Annals of Human Genetics|December 15, 2006
Congenital disorder of glycosylation type Ia: searching for the origin of common mutations in PMM2D Quelhas, R Quental, L Vilarinho, et al.
Annals of Human Genetics|November 14, 2006
The effects of SNP genotyping errors on the power of the Cochran-Armitage linear trend test for case/control association studiesKwangmi Ahn, Chad Haynes, Wonkuk Kim, et al.
Annals of Human Genetics|December 22, 2006
Carrier frequency of a nonsense mutation in the adenosine deaminase (ADA) gene implies a high incidence of ADA-deficient severe combined immunodeficiency (SCID) in Somalia and a single, common haplotype indicates common ancestryJuan J Sanchez, Gemma Monaghan, Claus Børsting, et al.
Annals of Human Genetics|December 2, 2008
Association of a polymorphism in the intron 7 of the SREBF1 gene with osteonecrosis of the femoral head in KoreansH-J Lee, S-J Choi, J M Hong, et al.
Annals of Human Genetics|April 7, 2009
New mutations of EXT1 and EXT2 genes in German patients with Multiple OsteochondromasWolfram Heinritz, Ulrike Hüffmeier, Sibylle Strenge, et al.
Annals of Human Genetics|May 22, 2009
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1Deqiong Ma, Daria Salyakina, James M Jaworski, et al.
Annals of Human Genetics|May 22, 2009
Revisiting MSUD in Portuguese Gypsies: evidence for a founder mutation and for a mutational hotspot within the BCKDHA geneSofia Quental, Alfredo Gusmão, Pilar Rodríguez-Pombo, et al.
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