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Article

Three patients with different phenotypes in a family with chromosome 22q11.2 deletions.

Pediatrics international : official journal of the Japan Pediatric Society - 1 Apr 2000

Akiba T, Odake A, Shirahata E, Matsunaga A, Sakamoto M, Yazaki N

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 10804739
DOI: 10.1046/j.1442-200x.2000.01183.x

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