A faster strategy for prenatal diagnosis of fragile X syndrome

被引：1

作者：

Schmitt, S. ^{[1
]}

Giraud, M. ^{[1
]}

Hary, J. ^{[1
]}

Rival, J. M. ^{[1
]}

Bezieau, S. ^{[1
,2
]}

Boisseau, P. ^{[1
]}

机构：

[1] CHU Nantes, Serv Genet Med, F-44093 Nantes 1, France

[2] Univ Nantes, Lab Biometadys, Fac Med, F-44035 Nantes, France

来源：

PRENATAL DIAGNOSIS | 2010年 / 30卷 / 12-13期

关键词：

DNA; fetal cells; nucleic acids and proteins; single gene disorders; genetic counselling; prenatal diagnosis; fragile X syndrome; FMRI; PREMUTATION;

D O I：

10.1002/pd.2617

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：1217 / 1219

页数：3

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