SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma
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| Description | scientific article (publication date: 15 October 2007) |
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author: Mariya Moosajee Donna S. Mackay Lourdes Santos-Pinto Neil Vargesson Agnès Bloch-Zupan Franz Rüschendorf |
| Publication date | October 15, 2007 |
| Language | English |
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