Whole-genome sequencing provides novel insights into the role of de novo mutations in male infertility

被引：0

作者：

Alzahrani, Shrooq ^{[1
]}

Franco, Cristina Diaz ^{[1
]}

Smith, Hannah ^{[1
]}

Oud, Manon ^{[2
]}

Alobaidi, Bilal ^{[1
]}

Coxhead, Jonathan ^{[3
]}

Mceleny, Kevin ^{[4
]}

Van der Heijden, Godfried ^{[5
]}

Batty, Lois ^{[1
]}

Ramos, Liliana ^{[5
]}

Xavier, Miguel ^{[1
]}

Veltman, Joris ^{[1
]}

机构：

[1] Newcastle Univ, Biosci Inst, Fac Med Sci, Newcastle Upon Tyne, Tyne & Wear, England

[2] Radboudumc, Donders Inst Brain Cognit & Behav, Dept Human Genet, Nijmegen, Netherlands

[3] Newcastle Univ, Genom Core Facil, Fac Med Sci, Newcastle Upon Tyne, Tyne & Wear, England

[4] Newcastle upon Tyne Hosp NHS Fdn Trust, Newcastle Fertil Ctr, Newcastle Upon Tyne, Tyne & Wear, England

[5] Radboudumc, Dept Obstet & Gynaecol, Nijmegen, Netherlands

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32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：

P01.030.B

引用

页码：358 / 358

页数：1

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