In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCNQ1OT gene

被引：383

作者：

Gicquel, C

Gaston, V

Mandelbaum, J

Siffroi, JP

Flahault, A

Le Bouc, Y

机构：

[1] Hosp Armand Trousseau, Lab Explorat Fonct Endocriniennes, F-75012 Paris, France

[2] Hosp Armand Trousseau, INSERM, U515, Paris, France

[3] Hop Tenon, Assistance Publ Hop Paris, Serv Histol Biol Reprod & Cytogenet, F-75970 Paris, France

[4] Hop Tenon, Assistance Publ Hop Paris, UPRES EA 1533, F-75970 Paris, France

[5] Hop Tenon, Assistance Publ Hop Paris, INSERM,U444, Unite Biostat, F-75970 Paris, France

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 2003年 / 72卷 / 05期

关键词：

D O I：

10.1086/374824

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：1338 / 1341

页数：4

共 23 条

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