Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies
Year: 2010
Type: article
Study design: Observational Study
Source: Journal of Human Genetics
DOI: 10.1038/jhg.2010.129
Authors: Shin Hayashi, Issei Imoto, Yoshinori Aizu, Nobuhiko Okamoto, Seiji Mizuno, Kenji Kurosawa, Nana Okamoto, Shozo Honda, Satoshi Araki, Shuki Mizutani, Hironao Numabe, Shinji Saitoh, Tomoki Kosho, Yoshimitsu Fukushima, Hiroshi Mitsubuchi, Fumio Endo, Yasutsugu Chinen, Rika Kosaki, Torayuki Okuyama, Hirotaka Ohki, Hiroshi Yoshihashi, Masae Ono, Fumio Takada, Hiroaki Ono, Mariko Yagi, Hiroshi Matsumoto, Yoshio Makita, Akira Hata, Johji Inazawa
Institutions: Tokyo Medical and Dental University, Tokushima University, BML (Japan), Osaka Women's and Children's Hospital, Aichi Human Service Center, Kanagawa Children's Medical Center, Kyoto University Hospital, Hokkaido University, Shinshu University, Shinshu University Hospital, Kumamoto University, University of the Ryukyus, National Center For Child Health and Development, Tokyo Metropolitan Children's Medical Center, Tokyo Teishin Hospital, Kitasato University, Hiroshima Prefectural Hospital, Kobe University, National Defense Medical College, Asahikawa Medical University, Chiba University
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
Awards: Pathophysilogy of brain dysfunction in Angelman and Prader-Willi syndrome., New diagnostic approach for malformation syndromes and genome-wide search for syndrome specific genome imbalance using DNA microarray, Development of array based comparative genomic hybridization (CGH) as a diagnostic tool for cryptic chromosome aberrations in congenital disorders, G6718509927, G8546646505
OpenAlex ID: W2149384116