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

页码：273 / 277

页数：5

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