Prenatal diagnosis of tetralogy of Fallot associated with chromosome 22q11 deletion.

Microdeletion of 22q11 is responsible for DiGeorge syndrome, velocardiofacial syndrome, congenital conotruncal heart defects, and related disorders. We report our experiences on prenatal diagnosis by fluorescence in situ hybridization (FISH) for 22q11 deletion in two fetuses with tetralogy of Fallot...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Oh, Dong Chul, Min, Jee Yeon, Lee, Moon Hee, Kim, Young Mi, Park, So Yeon, Won, Hea Sung, Kim, In Kyu, Lee, Young Ho, Yoo, Shi Joon, Ryu, Hyun Mee
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Korean Academy of Medical Sciences 2002
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3054817/
https://ncbi.nlm.nih.gov/pubmed/11850602
Etiketak: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Antzeko izenburuak