Facilitating variant curation sharing for fetal precision genomics: A new venture for prenatal diagnosis-Reference-Cited by-同舟云学术

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Facilitating variant curation sharing for fetal precision genomics: A new venture for prenatal diagnosis

Published:2022-11 Issue:12 Volume:42 Page:1479-1480
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Chitty Lyn S.¹²^ORCID,Van den Veyver Ignatia B.³⁴^ORCID

Affiliation:

1. North Thames Genomic Laboratory Hub Great Ormond Street NHS Foundation Trust London UK

2. Genetics and Genomics, UCL Great Ormond Street Institute of Child Health London UK

3. Departments of Obstetrics and Gynecology and Molecular and Human Genetics Baylor College of Medicine Houston TX USA

4. Texas Children's Hospital Houston TX USA

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.6252

Reference16 articles.

1. The many etiologies of nonimmune hydrops fetalis diagnosed by exome sequencing

2. Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study

3. Lessons learnt from prenatal exome sequencing

4. Evolving fetal phenotypes and clinical impact of progressive prenatal exome sequencing pathways: cohort study

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1. Lethal phenotypes in Mendelian disorders;Genetics in Medicine;2024-07

2. Lethal phenotypes in Mendelian disorders;2024-01-13

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