Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1):: Confirmation of the Mowat-Wilson syndrome

被引：42

作者：

Garavelli, L

Donadio, A

Zanacca, C

Banchini, G

Della Giustina, E

Bertani, G

Albertini, G

Del Rossi, C

Zweier, C

Rauch, A

Zollino, M

Neri, G

机构：

[1] Santa Maria Nuova Hosp, Div Pediat, Ambulatorio Genet Clin, Dept Pediat & Clin Genet, I-42100 Reggio Emilia, Italy

[2] Santa Maria Nuova Hosp, Dept Neuropsichiat, Reggio Emilia, Italy

[3] Santa Maria Nuova Hosp, Dept Dermatol, Reggio Emilia, Italy

[4] Parma Hosp, Dept Pediat Surg, Parma, Italy

[5] Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, Germany

[6] A Gemelli Catholic Univ Rome, Inst Med Genet, Rome, Italy

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2003年 / 116A卷 / 04期

关键词：

D O I：

10.1002/ajmg.a.10855

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：385 / 388

页数：4

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