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American Journal of Human Genetics logoLink to American Journal of Human Genetics
letter
. 1999 Aug;65(2):562–566. doi: 10.1086/302514

A 22q11.2 deletion that excludes UFD1L and CDC45L in a patient with conotruncal and craniofacial defects.

S C Saitta, J M McGrath, H Mensch, T H Shaikh, E H Zackai, B S Emanuel
PMCID: PMC1377955  PMID: 10417299

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