X-linked VACTERL-H caused by deletion of exon 3 in FANCB: A case report

被引：2
|
作者：
Watanabe, Norikazu [1 ]
Tsutsumi, Seiji [1 ]
Miyano, Yuki [2 ]
Sato, Hidenori [2 ]
Nagase, Satoru [1 ]
机构：
[1] Yamagata Univ, Fac Med, Inst Promot Med Sci Res, Dept Obstet & Gynecol, Yamagata, Japan
[2] Yamagata Univ, Fac Med, Inst Promot Med Sci Res, Genome Informat Unit, Yamagata, Japan
来源：
CONGENITAL ANOMALIES | 2018年 / 58卷 / 05期
关键词：
COMPLEMENTATION GROUP-B; HYDROCEPHALUS SYNDROME; MUTATION;
D O I：
10.1111/cga.12262
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
[No abstract available]
引用
收藏
页码：171 / 172
页数：2
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