MEHMO, a novel syndrome: assignment of disease locus to Xp21.1-p22.13

被引:13
作者
DeLozier-Blanchet, CD [1 ]
Haenggeli, CA
Bottani, A
机构
[1] Univ Hosp Geneva, Dept Obstet & Gynecol, Div Med Genet, Geneva, Switzerland
[2] Univ Hosp Geneva, Dept Pediat, Geneva, Switzerland
关键词
D O I
10.1038/sj.ejhg.5200364
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
引用
收藏
页码:621 / 622
页数:2
相关论文
共 3 条
[1]  
DELOZIER-BLANCHET C D, 1989, Journal de Genetique Humaine, V37, P353
[2]   MEHMO (mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly, obesity), a novel syndrome:: assignment of disease locus to Xp21.1-p22.13 [J].
Steinmüller, R ;
Steinberger, D ;
Müller, U .
EUROPEAN JOURNAL OF HUMAN GENETICS, 1998, 6 (03) :201-206
[3]  
Winter RM, 1996, LONDON DYSMORPHOLOGY