Deletion and duplication of 11p13-11p14: Reciprocal aberrations derived from a paternal insertion
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference23 articles.
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2. Microduplication 22q11.2, and emerging syndrome: Clinical, cytogenetic and molecular analysis of thirteen patients;Ensenauer;Am J Hum Genet,2003
3. Mosaic deletion 11p13 in a child with dopamine beta-hydroxylase deficiency-Case report and review of the literature;Erez;Am J Med Genet Part A,2010
4. A new growth chart for preterm babies: Babson and Benda's chart updated with recent data and a new format;Fenton;BMC Pediatr,2003
5. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder;Fernandez;J Med Genet,2010
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1. Characterization of Associated Nonclassical Phenotypes in Patients with Deletion in the WAGR Region Identified by Chromosomal Microarray: New Insights and Literature Review;Molecular Syndromology;2022-02-11
2. A familial pericentric inversion of chromosome 11 associated with a microdeletion of 163kb and microduplication of 288kb at 11p13 and 11q22.3 without aniridia or eye anomalies;American Journal of Medical Genetics Part A;2015-09-30
3. Molecular Genetics of Aniridia;eLS;2013-09-20
4. A de novo 11p13 Microduplication in a Patient with Some Features Invoking Silver-Russell Syndrome;Molecular Syndromology;2013
5. Aniridia;European Journal of Human Genetics;2012-06-13
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