Refining the critical region of the novel 19q13.11 microdeletion syndrome to 750 Kb
- PMID: 19487540
- DOI: 10.1136/jmg.2009.066910
Refining the critical region of the novel 19q13.11 microdeletion syndrome to 750 Kb
Comment on
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19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation.J Med Genet. 2009 Sep;46(9):635-40. doi: 10.1136/jmg.2008.062034. Epub 2009 Jan 6. J Med Genet. 2009. PMID: 19126570
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