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The 22q11.2 deletion in African-American patients: an underdiagnosed population?
Am J Med Genet A. 2005 Apr 30;134(3):242-6. doi: 10.1002/ajmg.a.30069.
Am J Med Genet A. 2005.
PMID: 15754359
Free PMC article.
Independent de novo 22q11.2 deletions in first cousins with DiGeorge/velocardiofacial syndrome.
Saitta SC, Harris SE, McDonald-McGinn DM, Emanuel BS, Tonnesen MK, Zackai EH, Seitz SC, Driscoll DA.
Saitta SC, et al. Among authors: tonnesen mk.
Am J Med Genet A. 2004 Jan 30;124A(3):313-7. doi: 10.1002/ajmg.a.20421.
Am J Med Genet A. 2004.
PMID: 14708107
Free PMC article.
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Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!
McDonald-McGinn DM, Tonnesen MK, Laufer-Cahana A, Finucane B, Driscoll DA, Emanuel BS, Zackai EH.
McDonald-McGinn DM, et al. Among authors: tonnesen mk.
Genet Med. 2001 Jan-Feb;3(1):23-9. doi: 10.1097/00125817-200101000-00006.
Genet Med. 2001.
PMID: 11339373
Free article.
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