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 *

152 related articles for article (PubMed ID: 12436038)

  • 41. Epilepsy and neurodevelopmental disorders of language.
    Pal DK
    Curr Opin Neurol; 2011 Apr; 24(2):126-31. PubMed ID: 21293269
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Intracellular distribution of a speech/language disorder associated FOXP2 mutant.
    Mizutani A; Matsuzaki A; Momoi MY; Fujita E; Tanabe Y; Momoi T
    Biochem Biophys Res Commun; 2007 Feb; 353(4):869-74. PubMed ID: 17196932
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Language features in a mother and daughter of a chromosome 7;13 translocation involving FOXP2.
    Tomblin JB; O'Brien M; Shriberg LD; Williams C; Murray J; Patil S; Bjork J; Anderson S; Ballard K
    J Speech Lang Hear Res; 2009 Oct; 52(5):1157-74. PubMed ID: 19797137
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Early neuroimaging markers of FOXP2 intragenic deletion.
    Liégeois FJ; Hildebrand MS; Bonthrone A; Turner SJ; Scheffer IE; Bahlo M; Connelly A; Morgan AT
    Sci Rep; 2016 Oct; 6():35192. PubMed ID: 27734906
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum.
    Manning MA; Cassidy SB; Clericuzio C; Cherry AM; Schwartz S; Hudgins L; Enns GM; Hoyme HE
    Pediatrics; 2004 Aug; 114(2):451-7. PubMed ID: 15286229
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Talk of genetics and vice versa.
    Pinker S
    Nature; 2001 Oct; 413(6855):465-6. PubMed ID: 11586336
    [No Abstract]   [Full Text] [Related]  

  • 47. The genetics of autism.
    Muhle R; Trentacoste SV; Rapin I
    Pediatrics; 2004 May; 113(5):e472-86. PubMed ID: 15121991
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. Human Genetics: The Evolving Story of FOXP2.
    Fisher SE
    Curr Biol; 2019 Jan; 29(2):R65-R67. PubMed ID: 30668952
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Chromosome 7q: where autism meets language disorder?
    Folstein SE; Mankoski RE
    Am J Hum Genet; 2000 Aug; 67(2):278-81. PubMed ID: 10889044
    [No Abstract]   [Full Text] [Related]  

  • 51. Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment.
    Bartlett CW; Flax JF; Logue MW; Smith BJ; Vieland VJ; Tallal P; Brzustowicz LM
    Hum Hered; 2004; 57(1):10-20. PubMed ID: 15133308
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Human speech- and reading-related genes display partially overlapping expression patterns in the marmoset brain.
    Kato M; Okanoya K; Koike T; Sasaki E; Okano H; Watanabe S; Iriki A
    Brain Lang; 2014 Jun; 133():26-38. PubMed ID: 24769279
    [TBL] [Abstract][Full Text] [Related]  

  • 53. What can mice tell us about Foxp2 function?
    French CA; Fisher SE
    Curr Opin Neurobiol; 2014 Oct; 28():72-9. PubMed ID: 25048596
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Axon guidance pathways served as common targets for human speech/language evolution and related disorders.
    Lei H; Yan Z; Sun X; Zhang Y; Wang J; Ma C; Xu Q; Wang R; Jarvis ED; Sun Z
    Brain Lang; 2017 Nov; 174():1-8. PubMed ID: 28692932
    [TBL] [Abstract][Full Text] [Related]  

  • 55. FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.
    Tolosa A; Sanjuán J; Dagnall AM; Moltó MD; Herrero N; de Frutos R
    BMC Med Genet; 2010 Jul; 11():114. PubMed ID: 20649982
    [TBL] [Abstract][Full Text] [Related]  

  • 56. The speech gene FOXP2 is not imprinted.
    Thomas AC; Frost JM; Ishida M; Vargha-Khadem F; Moore GE; Stanier P
    J Med Genet; 2012 Nov; 49(11):669-70. PubMed ID: 23033221
    [No Abstract]   [Full Text] [Related]  

  • 57. Evaluation of FOXP2 as an autism susceptibility gene.
    Wassink TH; Piven J; Vieland VJ; Pietila J; Goedken RJ; Folstein SE; Sheffield VC
    Am J Med Genet; 2002 Jul; 114(5):566-9. PubMed ID: 12116195
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2.
    Toma C; Hervás A; Torrico B; Balmaña N; Salgado M; Maristany M; Vilella E; Martínez-Leal R; Planelles MI; Cuscó I; del Campo M; Pérez-Jurado LA; Caballero-Andaluz R; de Diego-Otero Y; Pérez-Costillas L; Ramos-Quiroga JA; Ribasés M; Bayés M; Cormand B
    Psychiatr Genet; 2013 Apr; 23(2):82-5. PubMed ID: 23277129
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.
    Estruch SB; Graham SA; Chinnappa SM; Deriziotis P; Fisher SE
    J Neurodev Disord; 2016; 8():44. PubMed ID: 27933109
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Unravelling neurogenetic networks implicated in developmental language disorders.
    Vernes SC; Fisher SE
    Biochem Soc Trans; 2009 Dec; 37(Pt 6):1263-9. PubMed ID: 19909259
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.