TABLE OF CONTENTS
Volume 54, Issue 3 (March 2009)
Review
The genetic bases for non-syndromic hearing loss among Chinese FREE
Xiao Mei Ouyang, Denise Yan, Hui Jun Yuan, Dai Pu, Li Lin Du, Don Yi Han and Xue Zhong Liu
J Hum Genet 54: 131-140; advance online publication, February 6, 2009; doi:10.1038/jhg.2009.4
Original Articles
Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22–21.3
Muhammad Salman Chishti, Kwanghyuk Lee, Merry-Lynn McDonald, Muhammad Jawad Hassan, Muhammad Ansar, Wasim Ahmad and Suzanne M Leal
J Hum Genet 54: 141-144; advance online publication, February 20, 2009; doi:10.1038/jhg.2009.2
Mucolipidosis II and III alpha/beta: mutation analysis of 40 Japanese patients showed genotype–phenotype correlation
Takanobu Otomo, Takeshi Muramatsu, Tohru Yorifuji, Torayuki Okuyama, Hiroki Nakabayashi, Toshiyuki Fukao, Toshihiro Ohura, Makoto Yoshino, Akemi Tanaka, Nobuhiko Okamoto, Koji Inui, Keiichi Ozono and Norio Sakai
J Hum Genet 54: 145-151; advance online publication, February 6, 2009; doi:10.1038/jhg.2009.3
Genetic sequence variations of BRCA1-interacting genes AURKA, BAP1, BARD1 and DHX9 in French Canadian Families with high risk of breast cancer
Frédéric Guénard, Yvan Labrie, Geneviève Ouellette, Charles Joly Beauparlant and Francine Durocher INHERIT BRCAs
J Hum Genet 54: 152-161; advance online publication, February 6, 2009; doi:10.1038/jhg.2009.6
Testing the association of novel meta-analysis-derived diabetes risk genes with type II diabetes and related metabolic traits in Asian Indian Sikhs
Dharambir K Sanghera, Latonya Been, Lyda Ortega, Gurpreet S Wander, Narinder K Mehra, Christopher E Aston, John J Mulvihill and Sarju Ralhan
J Hum Genet 54: 162-168; advance online publication, February 27, 2009; doi:10.1038/jhg.2009.7
A practical case–control association test for detecting a susceptibility allele at a copy number variation locus
Jun Ohashi
J Hum Genet 54: 169-173; advance online publication, February 6, 2009; doi:10.1038/jhg.2009.8
Median network analysis of defectively sequenced entire mitochondrial genomes from early and contemporary disease studies
Hans-Jürgen Bandelt, Yong-Gang Yao, Claudio M Bravi, Antonio Salas and Toomas Kivisild
J Hum Genet 54: 174-181; advance online publication, March 13, 2009; doi:10.1038/jhg.2009.9
Molecular population genetics of SLC4A1 and Southeast Asian Ovalocytosis
Jason A Wilder, Jonathan A Stone, Elizabeth G Preston, Lauren E Finn, Hannah L Ratcliffe and Herawati Sudoyo
J Hum Genet 54: 182-187; advance online publication, February 20, 2009; doi:10.1038/jhg.2009.12
Short Communication
Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairment
Nele Hilgert, Kelly Monahan, Kiyoto Kurima, Cindy Li, Rick A Friedman, Andrew J Griffith and Guy Van Camp
J Hum Genet 54: 188-190; advance online publication, January 30, 2009; doi:10.1038/jhg.2009.1
