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A de novo cryptic 5p deletion and 9p duplication detected by subtelomeric MLPA in a boy with cri du chat syndrome.
Am J Med Genet A. 2011 Feb;155A(2):450-4. doi: 10.1002/ajmg.a.33458.
Am J Med Genet A. 2011.
PMID: 21271672
No abstract available.
Screening for the GJB2 c.-3170 G>A (IVS 1+1 G>A) mutation in Brazilian deaf individuals using multiplex ligation-dependent probe amplification.
da Silva-Costa SM, Coeli FB, Lincoln-de-Carvalho CR, Marques-de-Faria AP, Kurc M, Pereira T, Pomilio MC, Sartorato EL.
da Silva-Costa SM, et al. Among authors: lincoln de carvalho cr.
Genet Test Mol Biomarkers. 2009 Oct;13(5):701-4. doi: 10.1089/gtmb.2009.0025.
Genet Test Mol Biomarkers. 2009.
PMID: 19715470
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A de novo mutation in CYP21A2 gene in a case of in vitro fertilization.
Silva-Grecco RLD, de Paula Michelatto D, Lincoln-de-Carvalho CR, Henrique PP, da Cunha HM, Palandi-de-Mello M.
Silva-Grecco RLD, et al. Among authors: lincoln de carvalho cr.
Mol Genet Metab Rep. 2015 Nov 9;5:98-102. doi: 10.1016/j.ymgmr.2015.10.011. eCollection 2015 Dec.
Mol Genet Metab Rep. 2015.
PMID: 28649552
Free PMC article.
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