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The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective.
J Neurol Sci. 2021 Jan 15;420:117260. doi: 10.1016/j.jns.2020.117260. Epub 2020 Dec 3.
J Neurol Sci. 2021.
PMID: 33310205
Prenatal Diagnosis of Fragile X Syndrome in a Twin Pregnancy Complicated by a Complete Retraction.
Prawer Y, Hunter M, Cronin S, Ling L, Aliaga Vera S, Fahey M, Gelfand N, Oertel R, Bartlett E, Francis D, Godler D.
Prawer Y, et al. Among authors: gelfand n.
Genes (Basel). 2018 Jun 7;9(6):287. doi: 10.3390/genes9060287.
Genes (Basel). 2018.
PMID: 29880767
Free PMC article.
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