19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation. (Q51873485)
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scientific article published on 6 January 2009
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation. |
scientific article published on 6 January 2009 |
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19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation. (English)
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O Raoul
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H V Firth
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G Royer
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C Turleau
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A Bernheim
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L Willatt
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A Munnich
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M Vekemans
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V Cormier-Daire
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L Colleaux
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6 January 2009
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46
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9
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635-640
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