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Vendor : Nortel
Exam Code : 920-173
Exam Name : Nortel Contact Center Rls. 7.0 Technical(R) Support
Questions and Answers : 60 Q & A
Updated On : June 14, 2019
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Test Code : 920-173
Test Name : Nortel Contact Center Rls. 7.0 Technical(R) Support
Vendor Name : Nortel
Q&A : 60 Real Questions

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next-era DNA sequencing identifies novel gene variations and pathways involved in certain language impairment | 920-173 Real Questions and VCE Practice Test

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    Pagnamenta, A. T. et al. Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel possibility loci for autism and dyslexia. Biol Psychiatry 68, 320–328, doi: 10.1016/j.biopsych.2010.02.002 (2010).

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    Filges, I. et al. reduced expression by SETBP1 haploinsufficiency reasons developmental and expressive language delay indicating a phenotype diverse from Schinzel-Giedion syndrome. J Med Genet forty eight, 117–122, doi: 10.1136/jmg.2010.084582 (2011).

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    Ercan-Sencicek, A. G. et al. A balanced t(10;15) translocation in a male affected person with developmental language disorder. Eur J Med Genet 55, 128–131, doi: 10.1016/j.ejmg.2011.12.005 (2012).

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    Marseglia, G. et al. 372 kb microdeletion in 18q12.3 inflicting SETBP1 haploinsufficiency associated with gentle mental retardation and expressive speech impairment. Eur J Med Genet fifty five, 216–221, doi: 10.1016/j.ejmg.2012.01.005 (2012).

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    Thevenon, J. et al. 12p13.33 microdeletion together with ELKS/ERC1, a brand new locus associated with childhood apraxia of speech. Eur J Hum Genet 21, eighty two–88, doi: 10.1038/ejhg.2012.116 (2013).

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    Amarillo, I. E., Li, W. L., Li, X., Vilain, E. & Kantarci, S. De novo single exon deletion of AUTS2 in a affected person with speech and language disorder: a review of disrupted AUTS2 and additional proof for its position in neurodevelopmental problems. Am J Med Genet A 164A, 958–965, doi: 10.1002/ajmg.a.36393 (2014).

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