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Ectodermal dysplasia-like syndrome with mental retardation due to contiguous gene deletion: further clinical and molecular delineation of del(2q32) syndrome.
Am J Med Genet A. 2010 Jan;152A(1):111-7. doi: 10.1002/ajmg.a.33164.
Am J Med Genet A. 2010.
PMID: 20034071
High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters.
Chaste P, Betancur C, Gérard-Blanluet M, Bargiacchi A, Kuzbari S, Drunat S, Leboyer M, Bourgeron T, Delorme R.
Chaste P, et al. Among authors: kuzbari s.
Mol Autism. 2012 Jun 27;3(1):5. doi: 10.1186/2040-2392-3-5.
Mol Autism. 2012.
PMID: 22738402
Free PMC article.
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