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4. A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment. Lozano R; Vino A; Lozano C; Fisher SE; Deriziotis P Eur J Hum Genet; 2015 Dec; 23(12):1702-7. PubMed ID: 25853299 [TBL] [Abstract][Full Text] [Related]
5. Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder. Sollis E; Graham SA; Vino A; Froehlich H; Vreeburg M; Dimitropoulou D; Gilissen C; Pfundt R; Rappold GA; Brunner HG; Deriziotis P; Fisher SE Hum Mol Genet; 2016 Feb; 25(3):546-57. PubMed ID: 26647308 [TBL] [Abstract][Full Text] [Related]
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8. FOXP1 mutations cause intellectual disability and a recognizable phenotype. Le Fevre AK; Taylor S; Malek NH; Horn D; Carr CW; Abdul-Rahman OA; O'Donnell S; Burgess T; Shaw M; Gecz J; Bain N; Fagan K; Hunter MF Am J Med Genet A; 2013 Dec; 161A(12):3166-75. PubMed ID: 24214399 [TBL] [Abstract][Full Text] [Related]
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11. FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring. Lozano R; Gbekie C; Siper PM; Srivastava S; Saland JM; Sethuram S; Tang L; Drapeau E; Frank Y; Buxbaum JD; Kolevzon A J Neurodev Disord; 2021 Apr; 13(1):18. PubMed ID: 33892622 [TBL] [Abstract][Full Text] [Related]
12. A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome. Urreizti R; Damanti S; Esteve C; Franco-Valls H; Castilla-Vallmanya L; Tonda R; Cormand B; Vilageliu L; Opitz JM; Neri G; Grinberg D; Balcells S Sci Rep; 2018 Jan; 8(1):694. PubMed ID: 29330474 [TBL] [Abstract][Full Text] [Related]
13. [Clinical features and genetic analysis of three children with mental retardation, language impairment and autistic features due to de novo variants of FOXP1 gene]. Hua R; Xu X; Wu D; Yang L; Yuan J; Zhu J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Dec; 38(12):1194-1198. PubMed ID: 34839505 [TBL] [Abstract][Full Text] [Related]
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15. Whole genome sequencing identifies a de novo 2.1 Mb balanced paracentric inversion disrupting FOXP1 and leading to severe intellectual disability. Vuillaume ML; Cogné B; Jeanne M; Boland A; Ung DC; Quinquis D; Besnard T; Deleuze JF; Redon R; Bézieau S; Laumonnier F; Toutain A Clin Chim Acta; 2018 Oct; 485():218-223. PubMed ID: 29969624 [TBL] [Abstract][Full Text] [Related]
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18. FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability? Myers A; du Souich C; Yang CL; Borovik L; Mwenifumbo J; Rupps R; Study C; Lehman A; Boerkoel CF Am J Med Genet A; 2017 Dec; 173(12):3172-3181. PubMed ID: 28884888 [TBL] [Abstract][Full Text] [Related]
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