Mapping of a de novo unequal crossover causing a deletion of the steroid 21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB) gene -: art. no. e53

被引：13
作者：
Koppens, PFJ
Smeets, HJM
de Wijs, IJ
Degenhart, HJ
机构：
[1] Erasmus MC Sophia, Dept Paediat, Rotterdam, Netherlands
[2] Clin Genet Ctr Maastricht, Maastricht, Netherlands
[3] Univ Med Ctr Nijmegen, Dept Human Genet, Nijmegen, Netherlands
来源：
JOURNAL OF MEDICAL GENETICS | 2003年 / 40卷 / 05期
关键词：
D O I：
10.1136/jmg.40.5.e53
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页数：7
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