New insights into understanding the genetic basis of severe bilateral eye anomalies

被引：0

作者：

Bax, D. A. ^{[1
]}

Broadgate, S. ^{[1
]}

Chassaing, N. ^{[2
,3
]}

Calvas, P. ^{[2
,3
]}

Holt, R. ^{[1
]}

Ceroni, F. ^{[1
]}

Bunyan, D. ^{[4
]}

Hoffman, J. ^{[5
]}

Bruty, J. ^{[6
]}

McMullan, D. ^{[6
]}

Wallis, Y. ^{[6
]}

Griffiths, M. ^{[5
]}

Ragge, N. K. ^{[1
,5
]}

机构：

[1] Oxford Brookes Univ, Oxford, England

[2] Hop Purpan, Serv Genet Med, Toulouse, France

[3] Univ Toulouse, CNRS, FRE 3742, INSERM,UMR 1056, Toulouse, France

[4] Salisbury NHS Fdn Trust, Wessex Reg Genet Lab, Salisbury, Wilts, England

[5] Birmingham Womens Hosp NHS Fdn Trust, West Midlands Reg Clin Genet Serv & Birmingham Hl, Birmingham, W Midlands, England

[6] Birmingham Womens Hosp, West Midlands Reg Genet Lab, Birmingham, W Midlands, England

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2018年 / 26卷

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：

P02.04D

引用

页码：171 / 171

页数：1

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