Publication details
Identification of 2.3-Mb gene Locus for Congenital Aural Atresia in 18q22.3 Deletion: A Case Report Analysed by Comparative Genomic Hybridization
| Authors | |
|---|---|
| Year of publication | 2006 |
| Type | Article in Periodical |
| Magazine / Source | Otology and Neurotology |
| MU Faculty or unit | |
| 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. |
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