Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis-Reference-Cited by-同舟云学术

Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis

Published:2018-07 Issue:7 Volume:20 Page:745-753
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Boissel Sarah,Fallet-Bianco Catherine,Chitayat David,Kremer Valérie,Nassif Christina,Rypens Françoise,Delrue Marie-Ange,Dal Soglio Dorothée,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

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim2017173.pdf

Reference42 articles.

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