Characterization of the phenotype and definition of the deletion in a new patient with ring chromosome 22

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Bibliographic Details
Published in:American Journal of Medical Genetics Part A 2004, Vol.130A (2), p.196-199
Main Authors: Battini, R., Battaglia, A., Bertini, V., Cioni, G., Parrini, B., Rapalini, E., Simi, P., Tinelli, F., Valetto, A.
Format: Report
Language:English
Subjects:
22q13.3 deletion syndrome
chromosome aberration
language impairment
multiple congenital anomalies/mental retardation syndrome
ring chromosome 22 [r]
Online Access:Get full text
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ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.30276