Array comparative genomic hybridisation-based identification of two imbalances of chromosome 1p in a 9-year-old girl with a monosomy 1p36 related phenotype and a family history of learning difficulties: a case report

Array comparative genomic hybridisation-based identification of two imbalances of chromosome 1p in a 9-year-old girl with a monosomy 1p36 related phenotype and a family history of learning difficulties: a case report

<p>Abstract</p> <p>Introduction</p> <p>Monosomy 1p36 is one of the most common terminal deletion syndromes, with an approximate incidence of 1 in every 5000 live births. This syndrome is associated with several pronounced clinical features including characteristic facia...

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Bibliographic Details
Main Authors: Fitzgibbon Gregory J, Clayton-Smith Jill, Banka Siddharth, Hamilton Susan J, Needham Margaret M, Dore Jonathan K, Miller Jake T, Pawson Gareth D, Gaunt Lorraine
Format: Article
Language:English
Published: BMC 2008-11-01
Series:Journal of Medical Case Reports
Online Access:http://www.jmedicalcasereports.com/content/2/1/355

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http://www.jmedicalcasereports.com/content/2/1/355

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