bibliographic entry 6789756 [be/6789756]
https://w3id.org/oc/corpus/be/6789756

is a
content
  • Phelan, MC. Deletion 22q13.3 syndrome, Orphanet J Rare Dis, 2008, 3, 14, DOI: 10.1186/1750-1172-3-14, PMID: 18505557
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