Identification of 2.3-Mb gene Locus for Congenital Aural Atresia in 18q22.3 Deletion: A Case Report Analysed by Comparative Genomic Hybridization

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Authors	DOSTÁL Aleš NĚMEČKOVÁ Jitka GAILLYOVÁ Renata VRANOVÁ Vladimíra ŽEŽULKOVÁ Dita LEJSKA Mojmír ŠLAPÁK Ivo DOSTÁLOVÁ Zuzana KUGLÍK Petr
Year of publication	2006
Type	Article in Periodical
Magazine / Source	Otology and Neurotology
MU Faculty or unit	Faculty of Science
Citation
Field	Genetics and molecular biology
Keywords	conductive hearing loss; congenital aural atresia; 18q22.3 deletion; comparative genomic hybridization
Description	The study describes one 18q deletion syndrome clinical report analysed by comparative genomic hybridization with an overview of 19 other selected 18q deletion syndrome patients presenting congenital aural atresia from 18 published articles and one presented poster on 18q deletion syndrome.
Related projects:	Molecular basis of cell and tissue regulations