NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome -: art. no. e128

被引：57

作者：

Borck, G

Redon, R

Sanlaville, D

Rio, M

Prieur, M

Lyonnet, S

Vekemans, M

Carter, NP

Munnich, A

Colleaux, L

Cormier-Daire, V

机构：

[1] Hop Necker Enfants Malad, INSERM, U393, F-75015 Paris, France

[2] Hop Necker Enfants Malad, Dept Med Genet, F-75015 Paris, France

[3] Wellcome Trust Sanger Inst, Cambridge CB10 1SA, England

来源：

JOURNAL OF MEDICAL GENETICS | 2004年 / 41卷 / 12期

关键词：

D O I：

10.1136/jmg.2004.026666

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页数：6

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