Cite
HARVARD Citation
Malan, V. et al. (2009). 19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation. Journal of medical genetics. 46 (9), pp. 635-640. [Online].
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Malan, V. et al. (2009). 19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation. Journal of medical genetics. 46 (9), pp. 635-640. [Online].