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by Chikovani, M. et al.Tbilisi State Medical University, Department of pediatrics and adolescence medicine; Depatrment of Craniofacial surgery, GeorgiaTreatments can often correct many of the critical...

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by Milczuk, H.A. et al.Department of Otolaryngology-Head and Neck Surgery, Oregon Health and Science University, Portland 97239, USAVelocardiofacial syndrome patients may have comparable outcomes to...

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by Mlynarski, E.E. et al.Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.Am. J. Hum. Genet. 2015; 5:753-64[See paper]

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by Monks, S. et al. Adults with 22q11.2DS were genotyped for a number of COMT polymorphisms as well as the Ashkenazi risk haplotype.Schizophr. Res. 2014; 1-3:231-6[See paper]

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by Gao, S. et al.TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome.Hum. Mol....

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by Mlynarski, E.E. et al.Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome.Hum. Genet. 2016; 3:273-85[See paper]

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