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First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B
- Source :
- Human genetics and genomics advances : HGG advances 3(2), 100093 (2022). doi:10.1016/j.xhgg.2022.100093, HGG Advances, 3, 2, Human Genetics and Genomics Advances, 3(2):100093. Cell Press, HGG Advances, Vol 3, Iss 2, Pp 100093-(2022), HGG Advances, 3
- Publication Year :
- 2022
- Publisher :
- Elsevier BV, 2022.
-
Abstract
- Human genetics and genomics advances : HGG advances 3(2), 100093 (2022). doi:10.1016/j.xhgg.2022.100093<br />Published by Cell Press, Cambridge, Ma.
- Subjects :
- Genetics & Heredity
multifactorial diseases
HNF1B
Science & Technology
MUTATIONS
VACTERL ASSOCIATION
TRACHEA
Medizin
genome-wide association study (GWAS)
QH426-470
TRACHEOESOPHAGEAL FISTULA
Reconstructive and regenerative medicine Radboud Institute for Health Sciences [Radboudumc 10]
Reconstructive and regenerative medicine Radboud Institute for Molecular Life Sciences [Radboudumc 10]
embryonic structures
Genetics
EPIDEMIOLOGY
Molecular Medicine
CTNNA3
Life Sciences & Biomedicine
Medical Genetics
esophageal atresia (EA)
FOXF1/FOXC2/FOXL1
Genetics (clinical)
Medicinsk genetik
Subjects
Details
- ISSN :
- 26662477
- Volume :
- 3
- Database :
- OpenAIRE
- Journal :
- Human Genetics and Genomics Advances
- Accession number :
- edsair.doi.dedup.....fc79e5156791ca2e478e6413392d5904
- Full Text :
- https://doi.org/10.1016/j.xhgg.2022.100093