Temporal and occipital lobe features in children with hypochondroplasia/FGFR3 gene mutation

被引:0
|
作者
Cristina M. Philpott
Elysa Widjaja
Charles Raybaud
Helen M. Branson
Peter Kannu
Susan Blaser
机构
[1] The Hospital for Sick Children,Department of Neuroradiology
[2] The Hospital for Sick Children,Diagnostic Imaging
[3] The Hospital for Sick Children,Division of Clinical and Metabolic Genetics
来源
Pediatric Radiology | 2013年 / 43卷
关键词
FGFR3 gene mutation; Hypochondroplasia; Mesial temporal lobe; Hippocampal dysplasia; MRI; Children;
D O I
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学科分类号
摘要
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页码:1190 / 1195
页数:5
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