Genomic Study of Severe Fetal Anomalies and Discovery of GREB1L Mutations in Renal Agenesis-Reference-Cited by-同舟云学术

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Genomic Study of Severe Fetal Anomalies and Discovery of GREB1L Mutations in Renal Agenesis

Published:2018-12 Issue:12 Volume:73 Page:677-679
ISSN:1533-9866
Container-title:Obstetrical & Gynecological Survey
language:en
Short-container-title:

Author:

Boissel Sarah,Fallet-Bianco Catherine,Chitayat David,Kremer Valérie,Nassif Christina,Rypens Françoise,Delrue Marie-Ange,Soglio Dorothée Dal,Oligny Luc L.,Patey Natalie,Flori Elisabeth,Cloutier Mireille,Dyment David,Campeau Philippe,Karalis Aspasia,Nizard Sonia,Fraser William D.,Audibert François,Lemyre Emmanuelle,Rouleau Guy A.,Hamdan Fadi F.,Kibar Zoha,Michaud Jacques L.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Obstetrics and Gynecology,General Medicine

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A single center experience of prenatal parent‐fetus trio exome sequencing for pregnancies with congenital anomalies;Prenatal Diagnosis;2022-05-20

2. Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges—Systematic Review of the Literature and Meta-Analysis;Diagnostics;2022-02-23

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