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MOLECULAR DEFINITION OF THE 11P15.5 REGION INVOLVED IN BECKWITH-WIEDEMANN SYNDROME AND PROBABLY IN PREDISPOSITION TO ADRENOCORTICAL CARCINOMA

被引：91
作者：
HENRY, I
JEANPIERRE, M
COUILLIN, P
BARICHARD, F
SERRE, JL
JOURNEL, H
LAMOUROUX, A
TURLEAU, C
DEGROUCHY, J
JUNIEN, C
机构：
[1] INSERM, U73, CHATEAU LONGCHAMP, BOIS BOULOGNE, F-75016 PARIS, FRANCE
[2] HOP PONCHAILLOU, SERV PEDIAT, F-35000 RENNES, FRANCE
[3] HOP NECKER ENFANTS MALAD, INSERM, U173, F-75730 PARIS, FRANCE
[4] HOP COCHIN, INSERM, U129, F-75674 PARIS 14, FRANCE
[5] CNRS, NEUROBIOL LAB, F-91190 GIF SUR YVETTE, FRANCE
来源：
HUMAN GENETICS | 1989年 / 81卷 / 03期
关键词：
D O I：
10.1007/BF00279003
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：273 / 277
页数：5
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