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Human Genetics|August 11, 2007
Genotype-phenotype correlations for SLC26A4-related deafnessHela Azaiez, Tao Yang, Sai Prasad, et al.Human Genetics|June 26, 2007
Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasisFrancesca Capon, Paola Di Meglio, Joanna Szaub, et al.Human Genetics|August 25, 2007
A most distant intergeneric hybrid offspring (Larcon) of lesser apes, Nomascus leucogenys and Hylobates larHirohisa Hirai, Yuriko Hirai, Hiroshi Domae, et al.Human Genetics|August 25, 2007
The first large duplication of the RSK2 gene identified in a Coffin-Lowry syndrome patientPatricia Marques Pereira, Delphine Heron, André HanauerHuman Genetics|August 25, 2007
Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesisAurore Carré, Mireille Castanet, Sylvia Sura-Trueba, et al.Human Genetics|June 15, 2007
Imprinting detection by extending a regression-based QTL analysis methodOlga Y Gorlova, Lei Lei, Dakai Zhu, et al.Human Genetics|December 1, 1991
Fine mapping of a human chromosome 6 ferritin heavy chain pseudogene: relevance to haemochromatosisK M Summers, K S Tam, P B Bartley, et al.Human Genetics|December 1, 1991
Low density lipoprotein receptor founder mutations in Afrikaner familial hypercholesterolaemic patients: a comparison of two geographical areasF Graadt van Roggen, D R van der Westhuyzen, A D Marais, et al.Human Genetics|May 16, 2007
Male-to-female sex reversal associated with an approximately 250 kb deletion upstream of NR0B1 (DAX1)Marta Smyk, Jonathan S Berg, Amber Pursley, et al.Human Genetics|August 1, 1991
Identification of mutations in two families with sporadic hemophilia AC Paynton, G Sarkar, S S SommerPageof 958