Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.
Burn J; Takao A; Wilson D; Cross I; Momma K; Wadey R; Scambler P; Goodship J; Journal Of Medical Genetics, 1993, vol. 30, issue 10, p 822, ISSN 00222593. ISBN 00222593.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef