A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome.
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| Title: | A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome. |
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| Authors: | Jensen M; Bioinformatics and Genomics Program, Pennsylvania State University, University Park, PA, USA., Kooy RF; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium., Simon TJ; Department of Psychiatry and Behavioral Sciences, School of Medicine, University of California Davis, Sacramento, CA, USA; MIND Institute, University of California Davis, Sacramento, CA, USA., Reyniers E; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium., Girirajan S; Bioinformatics and Genomics Program, Pennsylvania State University, University Park, PA, USA; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA, USA; Department of Anthropology, Pennsylvania State University, University Park, PA, USA., Tassone F; MIND Institute, University of California Davis, Sacramento, CA, USA; Department of Biochemistry and Molecular Medicine, University of California, Davis, Sacramento, CA, USA. Electronic address: ftassone@ucdavis.edu. |
| Source: | European journal of medical genetics [Eur J Med Genet] 2018 Apr; Vol. 61 (4), pp. 209-212. Date of Electronic Publication: 2017 Nov 28. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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