Art

J-GLOBAL ID：201302269851292946   Reference number：13A0755059

Clinical Phenotype and Candidate Genes for the 5q31.3 Microdeletion Syndrome

5q31.3微小欠失症候群における臨床表現型と候補遺伝子

Author (13)： HOSOKI Kana (Hokkaido Univ. Graduate School of Medicine, JPN) ,  OHTA Tohru (Health Sci. Univ. of Hokkaido, JPN) ,  NATSUME Jun (Nagoya Univ. Graduate School of Medicine, JPN) ,  IMAI Sumiko (Sagamino Social Insurance Hospital, JPN) ,  OKUMURA Akihisa (Juntendo Univ. School of Medicine, Tokyo, JPN) ,  MATSUI Takeshi (Clinical Lab. Center Mitsubishi Chemical Medience Corp., Nagasaki, JPN) ,  HARADA Naoki (Clinical Lab. Center Mitsubishi Chemical Medience Corp., Nagasaki, JPN) ,  BACINO Carlos A. (Baylor Coll. of Medicine and Texas Children’s Hospital Clinical Care Center, Texas) ,  SCAGLIA Fernando (Baylor Coll. of Medicine and Texas Children’s Hospital Clinical Care Center, Texas) ,  JONES Jeremy Y. (Baylor Coll. of Medicine and Texas Children’s Hospital, Texas, JPN) ,  NIIKAWA Norio (Health Sci. Univ. of Hokkaido, JPN) ,  SAITOH Shinji (Hokkaido Univ. Graduate School of Medicine, JPN) ,  SAITOH Shinji (Nagoya Univ. Graduate School of Medicine, JPN)
Material： American Journal of Medical Genetics. Part A  (Am J Med Genet Part A)
Volume： 158  Issue： 8  Page： 1891-1896  Publication year： Aug. 2012 
JST Material Number： E0725C  ISSN： 1552-4825  Document type： Article
Country of issue： United States (USA)  Language： ENGLISH (EN)

Terms in the title (4)： 微小欠失 ,  症候群 ,  臨床表現型 ,  候補遺伝子