Chromosome 22q11 microdeletions in tetralogy of Fallot.

Chromosome 22q11 fluorescence in situ hybridisation (FISH) studies were performed on 33 consecutive individuals attending a paediatric cardiology clinic with tetralogy of Fallot. Seven children had 22q11 microdeletions but only four had other clinical features associated with the newly recognised ch...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: Trainer, A H, Morrison, N, Dunlop, A, Wilson, N, Tolmie, J
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1996
Soggetti:
Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1511583/
https://ncbi.nlm.nih.gov/pubmed/8660052
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi