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Items: 1 to 20 of 129

1.

A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3.

Addis L, Friederici AD, Kotz SA, Sabisch B, Barry J, Richter N, Ludwig AA, Rübsamen R, Albert FW, Pääbo S, Newbury DF, Monaco AP.

Genes Brain Behav. 2010 Aug;9(6):545-61. doi: 10.1111/j.1601-183X.2010.00583.x.

3.
4.

Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population.

Villanueva P, Newbury DF, Jara L, De Barbieri Z, Mirza G, Palomino HM, Fernández MA, Cazier JB, Monaco AP, Palomino H.

Eur J Hum Genet. 2011 Jun;19(6):687-95. doi: 10.1038/ejhg.2010.251.

5.

A major susceptibility locus for specific language impairment is located on 13q21.

Bartlett CW, Flax JF, Logue MW, Vieland VJ, Bassett AS, Tallal P, Brzustowicz LM.

Am J Hum Genet. 2002 Jul;71(1):45-55.

6.

Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits.

Bates TC, Luciano M, Medland SE, Montgomery GW, Wright MJ, Martin NG.

Behav Genet. 2011 Jan;41(1):50-7. doi: 10.1007/s10519-010-9402-9.

PMID:
20949370
7.

Identification of candidate regions for a novel Usher syndrome type II locus.

Ben Rebeh I, Benzina Z, Dhouib H, Hadjamor I, Amyere M, Ayadi L, Turki K, Hammami B, Kmiha N, Kammoun H, Hakim B, Charfedine I, Vikkula M, Ghorbel A, Ayadi H, Masmoudi S.

Mol Vis. 2008 Sep 19;14:1719-26.

8.

Exclusion of an extracolonic disease modifier locus on chromosome 1p33-36 in a large Swiss familial adenomatous polyposis kindred.

Plasilova M, Russell AM, Wanner A, Wolf A, Dobbie Z, Müller HJ, Heinimann K.

Eur J Hum Genet. 2004 May;12(5):365-71.

9.

Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia.

Watkins KE, Dronkers NF, Vargha-Khadem F.

Brain. 2002 Mar;125(Pt 3):452-64.

10.

Developmental dyslexia: an update on genes, brains, and environments.

Grigorenko EL.

J Child Psychol Psychiatry. 2001 Jan;42(1):91-125. Review.

PMID:
11205626
11.

Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family.

Zhang Q, Guo X, Xiao X, Yi J, Jia X, Hejtmancik JF.

Mol Vis. 2004 Nov 17;10:890-900.

12.

Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.

Holliday EG, McLean DE, Nyholt DR, Mowry BJ.

Arch Gen Psychiatry. 2009 Oct;66(10):1058-67. doi: 10.1001/archgenpsychiatry.2009.136.

PMID:
19805696
13.

Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?

Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C.

Neurology. 2008 Feb 26;70(9):686-94.

PMID:
18032746
14.

Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36.

Field LL, Shumansky K, Ryan J, Truong D, Swiergala E, Kaplan BJ.

Genes Brain Behav. 2013 Feb;12(1):56-69. doi: 10.1111/gbb.12003.

15.

Endophenotypes of FOXP2: dysfunction within the human articulatory network.

Liégeois F, Morgan AT, Connelly A, Vargha-Khadem F.

Eur J Paediatr Neurol. 2011 Jul;15(4):283-8. doi: 10.1016/j.ejpn.2011.04.006.

PMID:
21576028
16.

Autosomal dominant moyamoya disease maps to chromosome 17q25.3.

Mineharu Y, Liu W, Inoue K, Matsuura N, Inoue S, Takenaka K, Ikeda H, Houkin K, Takagi Y, Kikuta K, Nozaki K, Hashimoto N, Koizumi A.

Neurology. 2008 Jun 10;70(24 Pt 2):2357-63. doi: 10.1212/01.wnl.0000291012.49986.f9.

PMID:
18463369
17.

Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.

Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA.

Mol Psychiatry. 2007 Apr;12(4):376-84.

PMID:
17179998
18.

Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci.

Burdon KP, Coster DJ, Charlesworth JC, Mills RA, Laurie KJ, Giunta C, Hewitt AW, Latimer P, Craig JE.

Hum Genet. 2008 Nov;124(4):379-86. doi: 10.1007/s00439-008-0555-z.

PMID:
18795334
19.

Autosomal dominant partial epilepsy with auditory features: a new locus on chromosome 19q13.11-q13.31.

Bisulli F, Naldi I, Baldassari S, Magini P, Licchetta L, Castegnaro G, Fabbri M, Stipa C, Ferrari S, Seri M, Gonçalves Silva GE, Tinuper P, Pippucci T.

Epilepsia. 2014 Jun;55(6):841-8. doi: 10.1111/epi.12560.

20.

A genome-wide scan maps a novel autosomal dominant juvenile-onset open-angle glaucoma locus to 2p15-16.

Lin Y, Liu T, Li J, Yang J, Du Q, Wang J, Yang Y, Liu X, Fan Y, Lu F, Chen Y, Pu Y, Zhang K, He X, Yang Z.

Mol Vis. 2008 Apr 18;14:739-44.

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