Llwytho...
Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects
Genomic disorders and rare copy number abnormalities are identified in 15–25% of patients with syndromic conditions, but their prevalence in individuals with isolated birth defects is less clear. A spectrum of congenital heart defects (CHDs) is seen in heterotaxy, a highly heritable and genetically...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Philos Trans R Soc Lond B Biol Sci |
|---|---|
| Prif Awduron: | , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
The Royal Society
2016
|
| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5104505/ https://ncbi.nlm.nih.gov/pubmed/27821535 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1098/rstb.2015.0406 |
| Tagiau: |
Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
|