Clinical and Molecular Characterization of a Patient With a Combination of a Deletion and a Duplication of 22q13 Using Array CGH

The Application of Clinical Genetics- New Zealand

doi 10.2147/tacg.s35799

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Date

September 1, 2012

Authors

Isabel Ochando

Publisher

Informa UK Limited

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Amanote Research

Clinical and Molecular Characterization of a Patient With a Combination of a Deletion and a Duplication of 22q13 Using Array CGH

The Application of Clinical Genetics- New Zealand

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Combined 22q11.1-Q11.21 Deletion With 15q11.2-Q13.3 Duplication Identified by Array-CGH in a 6 Years Old Boy

Use of Array CGH for Molecular Characterization of Genetic Disorders

Phenotypic and Genetic Characterization of a Patient With a De Novo Interstitial 14q24.1q24.3 Deletion

Clinical and Genomic Evaluation of a Chinese Patient With a Novel Deletion Associated With Phelan–McDermid Syndrome

MET Is a Potential Target Across All Papillary Renal Cell Carcinomas: Result From a Large Molecular Study of pRCC With CGH Array and Matching Gene Expression Array

A Sibship With Duplication of Xq28 Inherited From the Mother; Genomic Characterization and Clinical Outcomes

Prenatal Diagnosis and Molecular Cytogenetic Characterization of a De Novo Duplication of 15q24.3-Q26.1

Comprehensive Analysis of Wolf–Hirschhorn Syndrome Using Array CGH Indicates a High Prevalence of Translocations

Screening of the 1 Mb SOX9 5' Control Region by Array CGH Identifies a Large Deletion in a Case of Campomelic Dysplasia With XY Sex Reversal