TABLE OF CONTENTS
Volume 52, Issue 1 (January 2007)
Mini Reviews
Recent progress in genetics of Marfan syndrome and Marfan-associated disorders
Takeshi Mizuguchi and Naomichi Matsumoto
J Hum Genet 52: 1-12; advance online publication, October 24, 2007; doi:10.1007/s10038-006-0078-1
The NR4A nuclear receptor family in eosinophils
Ryoichi Hashida, Naganari Ohkura, Hirohisa Saito and Gozoh Tsujimoto
J Hum Genet 52: 13-20; advance online publication, November 10, 2007; doi:10.1007/s10038-006-0085-2
Original Articles
Identification and characterization of different SHOX gene deletions in patients with Leri–Weill dyschondrosteosys by MLPA assay
Valentina Gatta, Ivana Antonucci, Elisena Morizio, Chiara Palka, Rita Fischetto, Vahe Mokini, Stefano Tumini, Giuseppe Calabrese and Liborio Stuppia
J Hum Genet 52: 21-27; advance online publication, November 8, 2007; doi:10.1007/s10038-006-0074-5
Alpha-adrenoceptor gene variants and autonomic nervous system function in a young healthy Japanese population
Tetsuro Matsunaga, Koichiro Yasuda, Tetsuya Adachi, Ning Gu, Tsubasa Yamamura, Toshio Moritani, Gozoh Tsujimoto and Kinsuke Tsuda
J Hum Genet 52: 28-37; advance online publication, October 31, 2007; doi:10.1007/s10038-006-0076-3
MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome
Mei-rong Li, Hong Pan, Xin-Hua Bao, Yu-Zhi Zhang and Xi-Ru Wu
J Hum Genet 52: 38-47; advance online publication, November 7, 2007; doi:10.1007/s10038-006-0079-0
Mutation and haplotype analyses of the MUT gene in Japanese patients with methylmalonic acidemia
Osamu Sakamoto, Toshihiro Ohura, Yoichi Matsubara, Masaki Takayanagi and Shigeru Tsuchiya
J Hum Genet 52: 48-55; advance online publication, October 31, 2007; doi:10.1007/s10038-006-0077-2
Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential
Peter Bross, Zhijie Li, Jakob Hansen, Jens Jacob Hansen, Marit Nyholm Nielsen, Thomas Juhl Corydon, Costa Georgopoulos, Debbie Ang, Jytte Banner Lundemose, Klary Niezen-Koning, Hans Eiberg, Huanming Yang, Steen Kølvraa, Lars Bolund and Niels Gregersen
J Hum Genet 52: 56-65; advance online publication, October 27, 2007; doi:10.1007/s10038-006-0080-7
ADAM33 polymorphisms are associated with aspirin-intolerant asthma in the Japanese population
Takuro Sakagami, Nobuyoshi Jinnai, Toshiaki Nakajima, Takashi Sekigawa, Takashi Hasegawa, Eiichi Suzuki, Ituro Inoue and Fumitake Gejyo
J Hum Genet 52: 66-72; advance online publication, October 24, 2007; doi:10.1007/s10038-006-0081-6
Different roles of MTHFR C677T and A1298C polymorphisms in colorectal adenoma and colorectal cancer: a meta-analysis
Yan Huang, Shizhong Han, Yao Li, Yumin Mao and Yi Xie
J Hum Genet 52: 73-85; advance online publication, November 7, 2007; doi:10.1007/s10038-006-0082-5
Association and synergistic interaction between promoter variants of the DRD4 gene in Japanese schizophrenics
Mizuho Nakajima, Eiji Hattori, Kazuo Yamada, Yoshimi Iwayama, Tomoko Toyota, Yasuhide Iwata, Kenji J Tsuchiya, Genichi Sugihara, Kenji Hashimoto, Hiroyuki Watanabe, Masaomi Iyo, Akinori Hoshika and Takeo Yoshikawa
J Hum Genet 52: 86-91; advance online publication, November 7, 2007; doi:10.1007/s10038-006-0084-3
Allelic homogeneity in Avellino corneal dystrophy due to a founder effect
Kaoru Tsujikawa, Motokazu Tsujikawa, Hitoshi Watanabe, Naoyuki Maeda, Yoshitsugu Inoue, Takashi Fujikado and Yasuo Tano
J Hum Genet 52: 92-97; advance online publication, November 10, 2007; doi:10.1007/s10038-006-0083-4
Short Communication
DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray: standardization of molecular investigations of genetic diseases due to consanguinity
Ching-Wan Lam, Sui-Fan Tong, Keong Wong, Y F Luo, Hoi-Yin Tang, Shau-Yin Ha and Michael Ho-Ming Chan
J Hum Genet 52: 98-101; advance online publication, October 11, 2007; doi:10.1007/s10038-006-0075-4
