206 related articles for article (PubMed ID: 29463886)
21. Breakpoint localization using array-CGH in three siblings with an unbalanced 4q;16q translocation and childhood apraxia of speech (CAS).
Shriberg LD; Jakielski KJ; El-Shanti H
Am J Med Genet A; 2008 Sep; 146A(17):2227-33. PubMed ID: 18671280
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.
Fedorenko E; Morgan A; Murray E; Cardinaux A; Mei C; Tager-Flusberg H; Fisher SE; Kanwisher N
Eur J Hum Genet; 2016 Feb; 24(2):302-6. PubMed ID: 26173965
[TBL] [Abstract][Full Text] [Related]
24. Transcription factor 19 interacts with histone 3 lysine 4 trimethylation and controls gluconeogenesis via the nucleosome-remodeling-deacetylase complex.
Sen S; Sanyal S; Srivastava DK; Dasgupta D; Roy S; Das C
J Biol Chem; 2017 Dec; 292(50):20362-20378. PubMed ID: 29042441
[TBL] [Abstract][Full Text] [Related]
25. Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum.
Takahashi K; Liu FC; Hirokawa K; Takahashi H
J Neurosci Res; 2003 Jul; 73(1):61-72. PubMed ID: 12815709
[TBL] [Abstract][Full Text] [Related]
26. Germline Chd8 haploinsufficiency alters brain development in mouse.
Gompers AL; Su-Feher L; Ellegood J; Copping NA; Riyadh MA; Stradleigh TW; Pride MC; Schaffler MD; Wade AA; Catta-Preta R; Zdilar I; Louis S; Kaushik G; Mannion BJ; Plajzer-Frick I; Afzal V; Visel A; Pennacchio LA; Dickel DE; Lerch JP; Crawley JN; Zarbalis KS; Silverman JL; Nord AS
Nat Neurosci; 2017 Aug; 20(8):1062-1073. PubMed ID: 28671691
[TBL] [Abstract][Full Text] [Related]
27. Assessment of the key regulatory genes and their Interologs for Turner Syndrome employing network approach.
Farooqui A; Tazyeen S; Ahmed MM; Alam A; Ali S; Malik MZ; Ali S; Ishrat R
Sci Rep; 2018 Jul; 8(1):10091. PubMed ID: 29973620
[TBL] [Abstract][Full Text] [Related]
28. Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment.
Palka C; Alfonsi M; Mohn A; Cerbo R; Guanciali Franchi P; Fantasia D; Morizio E; Stuppia L; Calabrese G; Zori R; Chiarelli F; Palka G
Pediatrics; 2012 Jan; 129(1):e183-8. PubMed ID: 22144704
[TBL] [Abstract][Full Text] [Related]
29. Aetiology of childhood apraxia of speech: A clinical practice update for paediatricians.
Morgan AT; Webster R
J Paediatr Child Health; 2018 Oct; 54(10):1090-1095. PubMed ID: 30294994
[TBL] [Abstract][Full Text] [Related]
30. Aerodynamic indices of velopharyngeal function in childhood apraxia of speech.
Sealey LR; Giddens CL
Clin Linguist Phon; 2010 Jun; 24(6):417-30. PubMed ID: 20136498
[TBL] [Abstract][Full Text] [Related]
31. Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2.
Shriberg LD; Ballard KJ; Tomblin JB; Duffy JR; Odell KH; Williams CA
J Speech Lang Hear Res; 2006 Jun; 49(3):500-25. PubMed ID: 16787893
[TBL] [Abstract][Full Text] [Related]
32. Mutations in the Chromatin Regulator Gene BRPF1 Cause Syndromic Intellectual Disability and Deficient Histone Acetylation.
Yan K; Rousseau J; Littlejohn RO; Kiss C; Lehman A; Rosenfeld JA; Stumpel CTR; Stegmann APA; Robak L; Scaglia F; Nguyen TTM; Fu H; Ajeawung NF; Camurri MV; Li L; Gardham A; Panis B; Almannai M; Sacoto MJG; Baskin B; Ruivenkamp C; Xia F; Bi W; ; ; Cho MT; Potjer TP; Santen GWE; Parker MJ; Canham N; McKinnon M; Potocki L; MacKenzie JJ; Roeder ER; Campeau PM; Yang XJ
Am J Hum Genet; 2017 Jan; 100(1):91-104. PubMed ID: 27939640
[TBL] [Abstract][Full Text] [Related]
33. A new MAPT deletion in a case of speech apraxia leading to corticobasal syndrome.
Mazzon G; Menichelli A; Fabretto A; Cattaruzza T; Manganotti P
Neurocase; 2018 Jun; 24(3):140-144. PubMed ID: 29969053
[TBL] [Abstract][Full Text] [Related]
34. Integrated Analysis of Genetic Abnormalities of the Histone Lysine Methyltransferases in Prostate Cancer.
Zhang Y; Yan L; Yao W; Chen K; Xu H; Ye Z
Med Sci Monit; 2019 Jan; 25():193-239. PubMed ID: 30616239
[TBL] [Abstract][Full Text] [Related]
35. BRG1 Governs Nanog Transcription in Early Mouse Embryos and Embryonic Stem Cells via Antagonism of Histone H3 Lysine 9/14 Acetylation.
Carey TS; Cao Z; Choi I; Ganguly A; Wilson CA; Paul S; Knott JG
Mol Cell Biol; 2015 Dec; 35(24):4158-69. PubMed ID: 26416882
[TBL] [Abstract][Full Text] [Related]
36. Neuroanatomical correlates of childhood apraxia of speech: A connectomic approach.
Fiori S; Guzzetta A; Mitra J; Pannek K; Pasquariello R; Cipriani P; Tosetti M; Cioni G; Rose SE; Chilosi A
Neuroimage Clin; 2016; 12():894-901. PubMed ID: 27882295
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome.
van der Spek J; den Hoed J; Snijders Blok L; Dingemans AJM; Schijven D; Nellaker C; Venselaar H; Astuti GDN; Barakat TS; Bebin EM; Beck-Wödl S; Beunders G; Brown NJ; Brunet T; Brunner HG; Campeau PM; Čuturilo G; Gilissen C; Haack TB; Hüning I; Husain RA; Kamien B; Lim SC; Lovrecic L; Magg J; Maver A; Miranda V; Monteil DC; Ockeloen CW; Pais LS; Plaiasu V; Raiti L; Richmond C; Rieß A; Schwaibold EMC; Simon MEH; Spranger S; Tan TY; Thompson ML; de Vries BBA; Wilkins EJ; Willemsen MH; Francks C; Vissers LELM; Fisher SE; Kleefstra T
Genet Med; 2022 Jun; 24(6):1283-1296. PubMed ID: 35346573
[TBL] [Abstract][Full Text] [Related]
39. Regulation of Nucleosome Architecture and Factor Binding Revealed by Nuclease Footprinting of the ESC Genome.
Hainer SJ; Fazzio TG
Cell Rep; 2015 Oct; 13(1):61-69. PubMed ID: 26411677
[TBL] [Abstract][Full Text] [Related]
40. Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech.
Peter B; Wijsman EM; Nato AQ; ; Matsushita MM; Chapman KL; Stanaway IB; Wolff J; Oda K; Gabo VB; Raskind WH
PLoS One; 2016; 11(4):e0153864. PubMed ID: 27120335
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]