Residual risks for chromosomal aberrations in patients with normal NIPS (non-invasive prenatal screening) - a retrospective study

被引：0

作者：

Iglesias, Adriana ^{[1
]}

Van Opstal, Diane ^{[1
]}

Thurik, Florentine ^{[1
]}

Drost, Mark ^{[1
]}

Weerts, Marjolein ^{[1
]}

Joosten, Marieke ^{[1
]}

Diderich, Karin ^{[1
]}

van der Schoot, Vyne ^{[1
]}

van den Born, Myrthe ^{[1
]}

Galjaard, Robert-Jan ^{[1
]}

de Weerd, Sabina ^{[2
]}

Dijkman, Anneke ^{[3
]}

Papatsonis, Dimitri ^{[4
]}

Cornette, Jerome ^{[5
]}

Galjaard, Sander ^{[5
]}

Knapen, Maarten ^{[5
]}

Prinsen, Krista ^{[5
]}

Go, Attie ^{[5
]}

Stuurman, Kyra ^{[1
]}

Srebniak, Malgorzata ^{[1
]}

机构：

[1] Erasmus MC Sophia Childrens Hosp, Clin Genet, Rotterdam, Netherlands

[2] Albert Schweitzer Hosp, Obstet & Gynecol, Dordrecht, Netherlands

[3] Reinier de Graaf Gasthuis Hosp, Obstet & Gynecol, Delft, Netherlands

[4] Amphia Hosp, Obstet & Gynecol, Breda, Netherlands

[5] Erasmus MC, Obstet & Gynecol, Rotterdam, 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：

P03.029.A

引用

页码：1315 / 1315

页数：1

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