Journal of Human Genetics - Table of Contents alert Volume 57 Issue 3

TABLE OF CONTENTS Volume 57, Issue 3 (March 2012) In this issue Commentaries Review Original Articles Short Communications Correspondence Corrigenda Also new AOP Advertisement Accelerate Your Next-Generation Sequencing Sample QC. The new Agilent 2200 TapeStation system offers researchers a new level of confidence in their sample and library quality control. Designed for scalability, speed and simplicity, the system provides results in approximately one minute per sample, even for 96 samples. Read about our special introductory offer and download free information kit now. Sign up for e-alerts Recommend to your library Web feed Subscribe Advertisement Visit the Medical Genomics Series Web Focus on Cardiovascular Disease The Journal of Human Genetics is proud to present the Medical Genomics Series Web Focus on Cardiovascular Disease - a collection of the latest original and review articles on cardiovascular diseases, such as myocardial infarction, stroke, atherosclerosis, aortic aneurysm, heart failure and hypertension. Access the Web Focus today!   Commentaries Top A commentary on Association of adiponectin polymorphism with cord blood adiponectin concentrations and intrauterine growth Sonir R Antonini J Hum Genet 2012 57: 157-158; advance online publication, January 5, 2012; 10.1038/jhg.2011.149 Full Text Commentary on the mutation spectrum of and founder effects affecting the PTS gene in East-Asian populations Haruo Shintaku J Hum Genet 2012 57: 159-160; advance online publication, February 16, 2012; 10.1038/jhg.2011.153 Full Text Review Top Common genetic factors for hematological traits in Humans Yukinori Okada and Yoichiro Kamatani J Hum Genet 2012 57: 161-169; advance online publication, January 26, 2012; 10.1038/jhg.2012.2 Abstract | Full Text Original Articles Top Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III Amira Mili, Ilhem Ben Charfeddine, Ons Mamaï, Wafa Cherif, Labiba Adala, Abdelbasset Amara, Serena Pagliarani, Sabrina Lucchiari, Abdelkarim Ayadi, Neji Tebib, Abdelaziz Harbi, Jihene Bouguila, Dorra H'Mida, Ali Saad, Khalifa Limem, G P Comi and Moez Gribaa J Hum Genet 2012 57: 170-175; advance online publication, November 17, 2011; 10.1038/jhg.2011.122 Abstract | Full Text Association of the MMP9 gene with childhood cedar pollen sensitization and pollinosis Hiroki Inoue, Yoichi Mashimo, Makiko Funamizu, Shuji Yonekura, Shigetoshi Horiguchi, Naoki Shimojo, Yoichi Kohno, Yoshitaka Okamoto, Akira Hata and Yoichi Suzuki J Hum Genet 2012 57: 176-183; advance online publication, January 12, 2012; 10.1038/jhg.2011.148 Abstract | Full Text Common variants of SLAMF1 and ITLN1 on 1q21 are associated with type 2 diabetes in Indian population Rubina Tabassum, Anubha Mahajan, Om Prakash Dwivedi, Ganesh Chauhan, Charles J Spurgeon, M V Kranthi Kumar, Saurabh Ghosh, S V Madhu, Sandeep K Mathur, Giriraj R Chandak, Nikhil Tandon and Dwaipayan Bharadwaj J Hum Genet 2012 57: 184-190; advance online publication, January 26, 2012; 10.1038/jhg.2011.150 Abstract | Full Text Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion Nana Okamoto, Shin Hayashi, Ayako Masui, Rika Kosaki, Izumi Oguri, Tomoko Hasegawa, Issei Imoto, Yoshio Makita, Akira Hata, Keiji Moriyama and Johji Inazawa J Hum Genet 2012 57: 191-196; advance online publication, January 19, 2012; 10.1038/jhg.2011.154 Abstract | Full Text A family of oculofaciocardiodental syndrome (OFCD) with a novel BCOR mutation and genomic rearrangements involving NHS Yukiko Kondo, Hirotomo Saitsu, Toshinobu Miyamoto, Kiyomi Nishiyama, Yoshinori Tsurusaki, Hiroshi Doi, Noriko Miyake, Na-Kyung Ryoo, Jeong Hun Kim, Young Suk Yu and Naomichi Matsumoto J Hum Genet 2012 57: 197-201; advance online publication, February 2, 2012; 10.1038/jhg.2012.4 Abstract | Full Text Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage Masato Obayashi, Kinya Ishikawa, Yuishin Izumi, Makoto Takahashi, Yusuke Niimi, Nozomu Sato, Osamu Onodera, Ryuji Kaji, Masatoyo Nishizawa and Hidehiro Mizusawa J Hum Genet 2012 57: 202-206; advance online publication, February 9, 2012; 10.1038/jhg.2012.5 Abstract | Full Text Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features Yuriko Yoneda, Hirotomo Saitsu, Mayumi Touyama, Yoshio Makita, Akie Miyamoto, Keisuke Hamada, Naohiro Kurotaki, Hiroaki Tomita, Kiyomi Nishiyama, Yoshinori Tsurusaki, Hiroshi Doi, Noriko Miyake, Kazuhiro Ogata, Kenji Naritomi and Naomichi Matsumoto J Hum Genet 2012 57: 207-211; advance online publication, February 2, 2012; 10.1038/jhg.2012.7 Abstract | Full Text Short Communications Top Spectra of BRCA1 and BRCA2 mutations in Korean patients with breast cancer: the importance of whole-gene sequencing Ja-Hyun Jang, Jeong Eon Lee, Min-Jung Kwon, Chang-Seok Ki, Jong-Won Kim, Seok Jin Nam and Jung-Hyun Yang J Hum Genet 2012 57: 212-215; advance online publication, January 5, 2012; 10.1038/jhg.2011.139 Abstract | Full Text Present Y chromosomes reveal the ancestry of Emperor CAO Cao of 1800 years ago Chuanchao Wang, Shi Yan, Zheng Hou, Wenqing Fu, Momiao Xiong, Sheng Han, Li Jin and Hui Li J Hum Genet 2012 57: 216-218; advance online publication, December 22, 2011; 10.1038/jhg.2011.147 Abstract | Full Text Correspondence Top Myotonic dystrophy type 2 is rare in the Japanese population Tohru Matsuura, Narihiro Minami, Hajime Arahata, Kinji Ohno, Koji Abe, Yukiko K Hayashi and Ichizo Nishino J Hum Genet 2012 57: 219-220; advance online publication, January 19, 2012; 10.1038/jhg.2011.152 Full Text Corrigenda Top Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III Amira Mili, Ilhem Ben Charfeddine, Ons Mama, Sonia Abdelhak, Labiba Adala, Abdelbasset Amara, Serena Pagliarani, Sabrina Lucchiarri, Abdelkarim Ayadi, Neji Tebib, Abdelaziz Harbi, Jihene Bouguila, Dorra H'Mida, Ali Saad, Khalifa Limem, G P Comi and Moez Gribaa J Hum Genet 2012 57: 221; 10.1038/jhg.2012.3 Full Text Spectra of BRCA1 and BRCA2 mutations in Korean patients with breast cancer: the importance of whole-gene sequencing Ja-Hyun Jang, Jeong Eon Lee, Min-Jung Kwon, Chang-Seok Ki, Jong-Won Kim, Seok Jin Nam and Jung-Hyun Yang J Hum Genet 2012 57: 222; 10.1038/jhg.2012.13 Full Text Advertisement THE GENETIC SIGNATURE OF VIOLENCE AGAINST WOMEN? 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