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[Partial monosomy 11q. A new case].

Authors
Type
Published Article
Journal
Annales de génétique
Publication Date
Volume
20
Issue
1
Pages
63–66
Identifiers
PMID: 302678
Source
Medline

Abstract

Partial monosomy 11q due to a de novo 11q231 leads to 11qter deletion was detected in a patient who died at seven days of age with most malformations characteristic of monosomy 11q, including trigonocephaly, facial dysmorphia, and congenital heart disease. In this as in most previously reported cases, the break point was at 11q231.

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