Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22–q24.1. Issue 5 (30th April 2004)

• Record Type: Journal Article
• Authors: Ishihara, N; Yamada, K; Yamada, Y; Miura, K; Kato, J; Kuwabara, N; Hara, Y; Kobayashi, Y; Hoshino, K; Nomura, Y; Mimaki, M; Ohya, K; Matsushima, M; Nitta, H; Tanaka, K; Segawa, M; Ohki, T; Ezoe, T; Kumagai, T; Onuma, A; Kuroda, T; Yoneda, M; Yamanaka, T; Saeki, M; Segawa, M; Saji, T; Nagaya, M; Wakamatsu, N
• Is Part Of: Journal of medical genetics. Volume 41:Issue 5(2004)
• Page Start: 387
• Page End: 393
• Publication Date: 2004-04-30
• Subjects: 2q22 -- deletion -- mental retardation -- ZFHX1B; GER, gastroesophageal reflux -- HSCR, Hirschsprung disease -- PAS, pulmonary artery sling -- PDA, patent ductus arteriosus -- TOF, tetralogy of Fallot; Medical genetics -- Periodicals; 616.042
• DOI: 10.1136/jmg.2003.016154
• Languages: English
• ISSNs: 1468-6244