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

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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]
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container_end_page 199
container_issue 2
container_start_page 196
container_title American Journal of Medical Genetics Part A
container_volume 130A
creator Battini, R.
Battaglia, A.
Bertini, V.
Cioni, G.
Parrini, B.
Rapalini, E.
Simi, P.
Tinelli, F.
Valetto, A.
description
doi_str_mv 10.1002/ajmg.a.30276
format report
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ispartof American Journal of Medical Genetics Part A, 2004, Vol.130A (2), p.196-199
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source Wiley-Blackwell Read & Publish Collection
subjects 22q13.3 deletion syndrome
chromosome aberration
language impairment
multiple congenital anomalies/mental retardation syndrome
ring chromosome 22 [r]
title Characterization of the phenotype and definition of the deletion in a new patient with ring chromosome 22
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