Facilitating variant curation sharing for fetal precision genomics: A new venture for prenatal diagnosis
Prenat Diagn
.
2022 Nov;42(12):1479-1480.
doi: 10.1002/pd.6252.
Epub 2022 Nov 3.
Authors
Lyn S Chitty
1
2
,
Ignatia B Van den Veyver
3
4
Affiliations
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.
PMID:
36281059
DOI:
10.1002/pd.6252
No abstract available
Publication types
Editorial
MeSH terms
Databases, Genetic*
Female
Genomics*
Humans
Pregnancy
Prenatal Diagnosis
Grants and funding
R01HD055651/National Institute of Child Health and Human Development