WES expands the mutational spectrum in patients with Silver-Russell syndrome features

被引：0

作者：

Meyer, R. ^{[1
]}

Begemann, M. ^{[1
]}

Huebner, C. ^{[1
]}

Dey, D. ^{[1
]}

Kuechler, A. ^{[2
]}

Elgizouli, M. ^{[2
]}

Kroisel, P. ^{[3
]}

Fekete, G. ^{[4
]}

Ambrozaityte, L. ^{[5
]}

Matuleviciene, A. ^{[5
]}

Elbracht, M. ^{[1
]}

Eggermann, T. ^{[1
]}

机构：

[1] Rhein Westfal TH Aachen, Inst Human Genet, Fac Med, Aachen, Germany

[2] Univ Hosp Essen, Inst Human Genet, Essen, Germany

[3] Med Univ Graz, Inst Human Genet, Graz, Austria

[4] Semmelweis Univ, Dept Pediat 2, Budapest, Hungary

[5] Vilnius Univ, Fac Med, Dept Human & Med Genet, Inst Biomed Sci, Vilnius, Lithuania

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2020年 / 28卷 / SUPPL 1期

关键词：

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：

P03.56.B

引用

页码：229 / 230

页数：2

共 50 条

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