PRENATAL EXCLUSION TESTING FOR HUNTINGTONS-DISEASE - A PROBLEM OF TOO MUCH INFORMATION

被引：14

作者：

MILLAN, FA

CURTIS, A

MENNIE, M

HOLLOWAY, S

BOXER, M

FAED, MJW

CRAWFORD, JW

LISTON, WA

BROCK, DJH

机构：

[1] UNIV EDINBURGH, WESTERN GEN HOSP, HUMAN GENET UNIT, EDINBURGH EH4 2XU, MIDLOTHIAN, SCOTLAND

[2] UNIV DUNDEE, NINEWELLS HOSP & MED SCH, DEPT OBSTET & GYNAECOL, DUNDEE DD1 9SY, SCOTLAND

[3] UNIV DUNDEE, NINEWELLS HOSP & MED SCH, DEPT PATHOL, HUMAN GENET LAB, DUNDEE DD1 9SY, SCOTLAND

[4] UNIV EDINBURGH, ROYAL EDINBURGH INFIRM, DEPT OBSTET & GYNAECOL, EDINBURGH EH10 5HF, MIDLOTHIAN, SCOTLAND

来源：

关键词：

D O I：

10.1136/jmg.26.2.83

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：83 / 85

页数：3

共 10 条

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