论文信息 - Absence of NOTCH2 and Hey2 mutations in a familial Alagille syndrome case with a novel frameshift mutation in JAG1

Absence of NOTCH2 and Hey2 mutations in a familial Alagille syndrome case with a novel frameshift mutation in JAG1

ELMSLIE FV, 1995, J MED GENET, V32, P264, DOI 10.1136-jmg.32.4.264; Fischer A, 2004, MAMM GENOME, V15, P711, DOI 10.1007-s00335-004-2389-x; Krantz Ian D., 1999, Current Opinion in Pediatrics, V11, P558, DOI 10.1097-00008480-199912000-00015; McCright B, 2002, DEVELOPMENT, V129, P1075; McDaniell R, 2006, AM J HUM GENET, V79, P169, DOI 10.1086-505332; Nabulsi MM, 2003, AM J MED GENET A, V116A, P342, DOI 10.1002-ajmg.a.10020; Sakata Y, 2006, J MOL CELL CARDIOL, V40, P267, DOI 10.1016-j.yjmcc.2005.09.006; Warthen DM, 2006, HUM MUTAT, V27, P436, DOI 10.1002-humu.20310; Xue YZ, 1999, HUM MOL GENET, V8, P723, DOI 10.1093-hmg-8.5.723

G. Nemer | Sara Al-Ghadban | F. Bitar | Inaam El‐Rassy | Jad Bou-Abdallah

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