Proximal interstitial deletion of 7q: A case report and review of the literature
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference25 articles.
1. Clinical and cytogenetic survey of 39 individuals with Prader-Labhart Willi syndrome;Butler;Am J Med Genet,1986
2. Parental origin of chromosome 15 deletion in Prader-Willi syndrome;Butler;Lancet,1983
3. Parental origin of de novo chromosome rearrangements;Chamberlin;Hum Genet,1980
4. Partial monosomy 7 with interstitial deletions in two infants with differing congenital abnormalities;d'A Crawfurd;J Med Genet,1979
5. Delezione interstiziale del braccio lungo del cromosoma 7 e sue correlazioni cliniche;Del;Pathologica,1983
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1. Oculofacial Manifestations of Chromosomal Aberrations;The Eye in Pediatric Systemic Disease;2017
2. Interstitial deletion of 7q22.1q31.1 in a boy with structural brain abnormality, cardiac defect, developmental delay, and dysmorphic features;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2016-04-20
3. Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region;American Journal of Medical Genetics Part A;2015-10-05
4. Prenatal diagnosis of a 7q21.13q22.1 deletion detected using high-resolution microarray;Obstetrics & Gynecology Science;2014
5. A novel interstitial microdeletion of 7q22.1-7q22.3 detected by array comparative genomic hybridization;American Journal of Medical Genetics Part A;2011-10-14
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