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Page 1
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families.
Genes (Basel). 2020 Nov 11;11(11):1329. doi: 10.3390/genes11111329.
Genes (Basel). 2020.
PMID: 33187236
Free PMC article.
A microdeletion at Xq22.2 implicates a glycine receptor GLRA4 involved in intellectual disability, behavioral problems and craniofacial anomalies.
Labonne JD, Graves TD, Shen Y, Jones JR, Kong IK, Layman LC, Kim HG.
Labonne JD, et al. Among authors: graves td.
BMC Neurol. 2016 Aug 9;16:132. doi: 10.1186/s12883-016-0642-z.
BMC Neurol. 2016.
PMID: 27506666
Free PMC article.
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