Prenatal diagnostic exome sequencing analysis in 207 fetuses with congenital CNS anomalies

被引：0

作者：

Kalanithy, Jeshurun Chiaran ^{[1
,2
]}

Thiele, Holger ^{[3
]}

Waffenschmidt, Lea ^{[4
]}

Stegmann, Jil D. ^{[2
,5
]}

Schneider, Sophia ^{[2
]}

Reutter, Heiko ^{[2
,6
,7
]}

Merz, Waltraut ^{[8
]}

Dworschak, Gabriel ^{[9
]}

机构：

[1] Univ Bonn, Inst Neuroanat, Fac Med, Bonn, Germany

[2] Univ Bonn, Inst Human Genet, Fac Med, Bonn, Germany

[3] Univ Cologne, Cologne Ctr Genom CCG, Cologne, Germany

[4] Friedrich Alexander Univ Erlangen Nurnberg, Dept Pediat & Adolescent Med, Erlangen, Germany

[5] Univ Bonn, Inst Anat & Cell Biol, Fac Med, Bonn, Germany

[6] Friedrich Alexander Univ Erlangen Nurnberg, Inst Human Genet, Erlangen, Germany

[7] Friedrich Alexander Univ Erlangen Nurnberg, Div Neonatol & Pediat Intens Care, Dept Pediat & Adolescent Med, Erlangen, Germany

[8] Univ Hosp Bonn, Dept Obstet & Prenatal Med, Bonn, Germany

[9] Univ Hosp Bonn, Dept Neuropediat, Bonn, Germany

来源：

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D O I：

暂无

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

P10.066.B

引用

页码：502 / 502

页数：1