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Year | Number of Results |
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2005 | 1 |
2006 | 1 |
2009 | 1 |
2010 | 1 |
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Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.
Am J Hum Genet. 2006 Feb;78(2):303-14. doi: 10.1086/500273. Epub 2005 Dec 29.
Am J Hum Genet. 2006.
PMID: 16400610
Free PMC article.
Detection of CHD7 deletions by MLPA in CHARGE syndrome patients with a less typical phenotype.
Wincent J, Schulze A, Schoumans J.
Wincent J, et al.
Eur J Med Genet. 2009 Jul-Aug;52(4):271-2. doi: 10.1016/j.ejmg.2009.02.005. Epub 2009 Feb 25.
Eur J Med Genet. 2009.
PMID: 19248844
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Mutations in the CHD7 gene: the experience of a commercial laboratory.
Bartels CF, Scacheri C, White L, Scacheri PC, Bale S.
Bartels CF, et al.
Genet Test Mol Biomarkers. 2010 Dec;14(6):881-91. doi: 10.1089/gtmb.2010.0101.
Genet Test Mol Biomarkers. 2010.
PMID: 21158681
Free PMC article.
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