A novel Fibroblast Growth Factor Receptor 2 (FGFR2) mutation associated with a mild Crouzon syndrome

被引：0
|
作者：
Locuratolo, N. [1 ]
Baffico, M. [2 ]
Baldi, M. [2 ]
Parisi, V. [3 ]
Micacchi, F. [1 ]
Angelucci, V. [1 ]
Beccaglia, M. Rojas [4 ]
Pirro, C. [1 ]
Fattapposta, F. [1 ]
机构：
[1] Univ Roma La Sapienza, Dept Sensorial Organs, I-00185 Rome, Italy
[2] Galliera Hosp, Genet Lab, Dept Genet Sci, Genoa, Italy
[3] GB Bietti Fdn IRCCS, Rome, Italy
[4] Univ Roma La Sapienza, Emergency Dept, I-00185 Rome, Italy
来源：
ARCHIVES ITALIENNES DE BIOLOGIE | 2011年 / 149卷 / 03期
关键词：
GENE CAUSE; CRANIOSYNOSTOSES; DIVERSITY; SPECTRUM; PFEIFFER; DOMAIN;
D O I：
暂无
中图分类号：
Q189 [神经科学];
学科分类号：
071006 ;
摘要：
引用
收藏
页码：313 / 317
页数：5
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