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...

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Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: Korean Academy of Medical Sciences 2002
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3054817/
https://ncbi.nlm.nih.gov/pubmed/11850602
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