← Evidence map

ArticleThe application of clinical genetics2012

Clinical and molecular characterization of a patient with a combination of a deletion and a duplication of 22q13 using array CGH.

Isabel Ochando et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

Not cited yet

Full record →Abstract, authors, funding and every citing paper · PMID 23776384