Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects. [electronic resource]

By: Contributor(s): Producer: 20020517Description: e16 p. digitalISSN:
  • 1468-6244
Subject(s): Online resources: In: Journal of medical genetics vol. 39
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Publication Type: Letter

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