These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 20571508)

  • 1. Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency.
    Carr CW; Moreno-De-Luca D; Parker C; Zimmerman HH; Ledbetter N; Martin CL; Dobyns WB; Abdul-Rahman OA
    Eur J Hum Genet; 2010 Nov; 18(11):1216-20. PubMed ID: 20571508
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis.
    Pariani MJ; Spencer A; Graham JM; Rimoin DL
    Eur J Med Genet; 2009; 52(2-3):123-7. PubMed ID: 19332160
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.
    Zeesman S; Nowaczyk MJ; Teshima I; Roberts W; Cardy JO; Brian J; Senman L; Feuk L; Osborne LR; Scherer SW
    Am J Med Genet A; 2006 Mar; 140(5):509-14. PubMed ID: 16470794
    [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]  

  • 6. 3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination.
    Palumbo O; D'Agruma L; Minenna AF; Palumbo P; Stallone R; Palladino T; Zelante L; Carella M
    Gene; 2013 Mar; 516(1):107-13. PubMed ID: 23287644
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.
    Vernes SC; MacDermot KD; Monaco AP; Fisher SE
    Eur J Hum Genet; 2009 Oct; 17(10):1354-8. PubMed ID: 19352412
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Three Japanese patients with 3p13 microdeletions involving FOXP1.
    Yamamoto-Shimojima K; Okamoto N; Matsumura W; Okazaki T; Yamamoto T
    Brain Dev; 2019 Mar; 41(3):257-262. PubMed ID: 30424912
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders.
    Sollis E; Deriziotis P; Saitsu H; Miyake N; Matsumoto N; Hoffer MJV; Ruivenkamp CAL; Alders M; Okamoto N; Bijlsma EK; Plomp AS; Fisher SE
    Hum Mutat; 2017 Nov; 38(11):1542-1554. PubMed ID: 28741757
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.
    Horn D; Kapeller J; Rivera-Brugués N; Moog U; Lorenz-Depiereux B; Eck S; Hempel M; Wagenstaller J; Gawthrope A; Monaco AP; Bonin M; Riess O; Wohlleber E; Illig T; Bezzina CR; Franke A; Spranger S; Villavicencio-Lorini P; Seifert W; Rosenfeld J; Klopocki E; Rappold GA; Strom TM
    Hum Mutat; 2010 Nov; 31(11):E1851-60. PubMed ID: 20848658
    [TBL] [Abstract][Full Text] [Related]  

  • 11. De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.
    Hamdan FF; Daoud H; Rochefort D; Piton A; Gauthier J; Langlois M; Foomani G; Dobrzeniecka S; Krebs MO; Joober R; Lafrenière RG; Lacaille JC; Mottron L; Drapeau P; Beauchamp MH; Phillips MS; Fombonne E; Rouleau GA; Michaud JL
    Am J Hum Genet; 2010 Nov; 87(5):671-8. PubMed ID: 20950788
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prospective investigation of FOXP1 syndrome.
    Siper PM; De Rubeis S; Trelles MDP; Durkin A; Di Marino D; Muratet F; Frank Y; Lozano R; Eichler EE; Kelly M; Beighley J; Gerdts J; Wallace AS; Mefford HC; Bernier RA; Kolevzon A; Buxbaum JD
    Mol Autism; 2017; 8():57. PubMed ID: 29090079
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Foxp1 expression is essential for sex-specific murine neonatal ultrasonic vocalization.
    Fröhlich H; Rafiullah R; Schmitt N; Abele S; Rappold GA
    Hum Mol Genet; 2017 Apr; 26(8):1511-1521. PubMed ID: 28204507
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Phenotype of FOXP2 haploinsufficiency in a mother and son.
    Rice GM; Raca G; Jakielski KJ; Laffin JJ; Iyama-Kurtycz CM; Hartley SL; Sprague RE; Heintzelman AT; Shriberg LD
    Am J Med Genet A; 2012 Jan; 158A(1):174-81. PubMed ID: 22106036
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1.
    Johnson TB; Mechels K; Anderson RH; Cain JT; Sturdevant DA; Braddock S; Pinz H; Wilson MA; Landsverk M; Roux KJ; Weimer JM
    Sci Rep; 2018 Nov; 8(1):16161. PubMed ID: 30385778
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Differential Song Deficits after Lentivirus-Mediated Knockdown of FoxP1, FoxP2, or FoxP4 in Area X of Juvenile Zebra Finches.
    Norton P; Barschke P; Scharff C; Mendoza E
    J Neurosci; 2019 Dec; 39(49):9782-9796. PubMed ID: 31641053
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders.
    Bacon C; Rappold GA
    Hum Genet; 2012 Nov; 131(11):1687-98. PubMed ID: 22736078
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Monoallelic expression of the human FOXP2 speech gene.
    Adegbola AA; Cox GF; Bradshaw EM; Hafler DA; Gimelbrant A; Chess A
    Proc Natl Acad Sci U S A; 2015 Jun; 112(22):6848-54. PubMed ID: 25422445
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 gene.
    Mutlu-Albayrak H; Karaer K
    Int J Pediatr Otorhinolaryngol; 2019 Feb; 117():179-181. PubMed ID: 30579078
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.