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Year | Number of Results |
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2014 | 1 |
2016 | 1 |
2024 | 0 |
PubMed (cited) for id: 300968
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De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations.
Am J Hum Genet. 2016 Feb 4;98(2):373-81. doi: 10.1016/j.ajhg.2015.12.015. Epub 2016 Jan 28.
Am J Hum Genet. 2016.
PMID: 26833328
Free PMC article.
Massively parallel sequencing of patients with intellectual disability, congenital anomalies and/or autism spectrum disorders with a targeted gene panel.
Brett M, McPherson J, Zang ZJ, Lai A, Tan ES, Ng I, Ong LC, Cham B, Tan P, Rozen S, Tan EC.
Brett M, et al.
PLoS One. 2014 Apr 1;9(4):e93409. doi: 10.1371/journal.pone.0093409. eCollection 2014.
PLoS One. 2014.
PMID: 24690944
Free PMC article.
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