Llwytho...
22q11.2 Deletions in Patients with Conotruncal Defects: Data from 1610 Consecutive Cases
BACKGROUND: The 22q11.2 deletion syndrome is characterized by multiple congenital anomalies including conotruncal cardiac defects. Identifying the patient with a 22q11.2 deletion (22q11del) can be challenging because many extracardiac features become apparent later in life. We sought to better defin...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Pediatr Cardiol |
|---|---|
| Prif Awduron: | , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2013
|
| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4339067/ https://ncbi.nlm.nih.gov/pubmed/23604262 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00246-013-0694-4 |
| Tagiau: |
Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
|