TABLE OF CONTENTS
Volume 52, Issue 6 (June 2007)
Original Articles
Genetic determination in onset age of wrist fracture
Donghai Xiong, Wei Wang, Yuan Chen, Hui Jiang and Hong-Wen Deng
J Hum Genet 52: 481-484; advance online publication, April 25, 2007; doi:10.1007/s10038-007-0141-6
An 11-bp duplication in the promoter region of the VHL gene in a patient with cerebellar hemangioblastoma and renal oncocytoma
Lucia Anna Muscarella, Raffaela Barbano, Bartolomeo Augello, Vincenza Formica, Lucia Micale, Leopoldo Zelante, Leonardo D'Agruma and Giuseppe Merla
J Hum Genet 52: 485-491; advance online publication, April 17, 2007; doi:10.1007/s10038-007-0138-1
Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum
Hao Hu, Lingqian Wu, Yong Feng, Qian Pan, Zhigao Long, Juan Li, Heping Dai, Kun Xia, Desheng Liang, Norio Niikawa and Jiahui Xia
J Hum Genet 52: 492-497; advance online publication, April 19, 2007; doi:10.1007/s10038-007-0139-0
Gap junction coding genes and schizophrenia: a genetic association study
Branko Aleksic, Ryoko Ishihara, Nagahide Takahashi, Nobuhisa Maeno, Xiaofei Ji, Shinichi Saito, Toshiya Inada and Norio Ozaki
J Hum Genet 52: 498-501; advance online publication, April 11, 2007; doi:10.1007/s10038-007-0142-5
Association of KIT gene polymorphisms with bone mineral density in postmenopausal Korean women
Shin-Yoon Kim, Jong-Young Lee, Ha Young Kim, Bermseok Oh, Kuchan Kimm, Hyung-Lae Kim, Byung Lae Park, Hyoung Doo Shin, Eui Kyun Park, Jung-Min Koh and Ghi Su Kim
J Hum Genet 52: 502-509; advance online publication, May 9, 2007; doi:10.1007/s10038-007-0143-4
Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese
Hisakuni Fukuoka, Yukihiko Kanda, Shuji Ohta and Shin-ichi Usami
J Hum Genet 52: 510-515; advance online publication, May 11, 2007; doi:10.1007/s10038-007-0144-3
The 894G>T variant in the endothelial nitric oxide synthase gene and spina bifida risk
Ivon J M van der Linden, Sandra G Heil, Martin den Heijer and Henk J Blom
J Hum Genet 52: 516-520; advance online publication, May 4, 2007; doi:10.1007/s10038-007-0147-0
Further evidence of genetic heterogeneity in Costello syndrome: involvement of the KRAS gene
Débora Romeo Bertola, Alexandre Costa Pereira, Amanda Salem Brasil, Lilian Maria José Albano, Chong Ae Kim and José Eduardo Krieger
J Hum Genet 52: 521-526; advance online publication, April 28, 2007; doi:10.1007/s10038-007-0146-1
Polymorphisms of glutathione S-transferase M1, T1 and P1 in patients with reflux esophagitis and Barrett's esophagus
Zdenek Kala, Ji
í Dolina, Filip Marek and Lydie Izakovicova Holla
J Hum Genet 52: 527-534; advance online publication, May 3, 2007; doi:10.1007/s10038-007-0148-z
Retinoblastoma and mental retardation microdeletion syndrome: clinical characterization and molecular dissection using array CGH
R Caselli, C Speciale, C Pescucci, V Uliana, K Sampieri, M Bruttini, I Longo, S De Francesco, T Pramparo, O Zuffardi, R Frezzotti, A Acquaviva, T Hadjistilianou, A Renieri and F Mari
J Hum Genet 52: 535-542; advance online publication, May 15, 2007; doi:10.1007/s10038-007-0151-4
Mutation of junctophilin type 2 associated with hypertrophic cardiomyopathy
Yoshihisa Matsushita, Toru Furukawa, Hiroshi Kasanuki, Makoto Nishibatake, Yachiyo Kurihara, Atsushi Ikeda, Naoyuki Kamatani, Hiroshi Takeshima and Rumiko Matsuoka
J Hum Genet 52: 543-548; advance online publication, May 3, 2007; doi:10.1007/s10038-007-0149-y
Short Communications
A novel DFNA5 mutation does not cause hearing loss in an Iranian family
Lut Van Laer, Nicole C Meyer, Mahdi Malekpour, Yasser Riazalhosseini, Mahdi Moghannibashi, Kimia Kahrizi, Ann Vandevelde, Fatemeh Alasti, Hossein Najmabadi, Guy Van Camp and Richard J H Smith
J Hum Genet 52: 549-552; advance online publication, April 11, 2007; doi:10.1007/s10038-007-0137-2
Mutation identification and characterization of a Taiwanese patient with fucosidosis
Shuan-Pei Lin, Jui-Hung Chang, Maria Paez de la Cadena, Ting-Fang Chang and Guey-Jen Lee-Chen
J Hum Genet 52: 553-556; advance online publication, April 11, 2007; doi:10.1007/s10038-007-0136-3
Failure to confirm association between PDCD1 polymorphisms and rheumatoid arthritis in a Japanese population
Takuji Iwamoto, Katsunori Ikari, Eisuke Inoue, Yoshiaki Toyama, Masako Hara, Hisashi Yamanaka, Taisuke Tomatsu, Shigeki Momohara and Naoyuki Kamatani
J Hum Genet 52: 557-560; advance online publication, April 28, 2007; doi:10.1007/s10038-007-0145-2
A syndactyly type IV locus maps to 7q36
Daisuke Sato, Desheng Liang, Lingqian Wu, Qian Pan, Kun Xia, Heping Dai, Hua Wang, Gen Nishimura, Koh-Ichiro Yoshiura, Jiahui Xia and Norio Niikawa
J Hum Genet 52: 561-564; advance online publication, May 3, 2007; doi:10.1007/s10038-007-0150-5
Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation
Jing Yu Liu, Xiang Ren, Xiufeng Yang, Tangying Guo, Qi Yao, Lin Li, Xiaohua Dai, Mingchang Zhang, Lejin Wang, Mugen Liu and Qing K Wang
J Hum Genet 52: 565-570; advance online publication, May 22, 2007; doi:10.1007/s10038-007-0152-3
