Works matching IS 13646745 AND DT 2010 AND VI 11 AND IP 3

Results: 10

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

Published in:

Neurogenetics, 2010, v. 11, n. 3, p. 291, doi. 10.1007/s10048-009-0228-7

By:

Cukier, Holly;
Rabionet, Raquel;
Konidari, Ioanna;
Rayner-Evans, Melissa;
Baltos, Mary;
Wright, Harry;
Abramson, Ruth;
Martin, Eden;
Cuccaro, Michael;
Pericak-Vance, Margaret;
Gilbert, John

Publication type:

Article

RNA processing pathways in amyotrophic lateral sclerosis.

Published in:

Neurogenetics, 2010, v. 11, n. 3, p. 275, doi. 10.1007/s10048-010-0239-4

By:

Blitterswijk, Marka;
Landers, John

Publication type:

Article

Analysis of exon dosage using MLPA in South African Parkinson's disease patients.

Published in:

Neurogenetics, 2010, v. 11, n. 3, p. 305, doi. 10.1007/s10048-009-0229-6

By:

Keyser, Rowena;
Lombard, Debbie;
Veikondis, Rene;
Carr, Jonathan;
Bardien, Soraya

Publication type:

Article

Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19.

Published in:

Neurogenetics, 2010, v. 11, n. 3, p. 313, doi. 10.1007/s10048-009-0230-0

By:

Meilleur, K.;
Traoré, M.;
Sangaré, M.;
Britton, A.;
Landouré, G.;
Coulibaly, S.;
Niaré, B.;
Mochel, F.;
Pean, A.;
Rafferty, I.;
Watts, C.;
Shriner, D.;
Littleton-Kearney, M.;
Blackstone, C.;
Singleton, A.;
Fischbeck, K.

Publication type:

Article

Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy.

Published in:

Neurogenetics, 2010, v. 11, n. 3, p. 319, doi. 10.1007/s10048-009-0232-y

By:

Kolb, Luis;
Arlier, Zulfikar;
Yalcinkaya, Cengiz;
Ozturk, Ali;
Moliterno, Jennifer;
Erturk, Ozdem;
Bayrakli, Fatih;
Korkmaz, Baris;
DiLuna, Michael;
Yasuno, Katsuhito;
Bilguvar, Kaya;
Ozcelik, Tayfun;
Tuysuz, Beyhan;
State, Matthew;
Gunel, Murat

Publication type:

Article

Molecular characterization of six Chinese families with m.3460G>A and Leber hereditary optic neuropathy.

Published in:

Neurogenetics, 2010, v. 11, n. 3, p. 349, doi. 10.1007/s10048-010-0236-7

By:

Yu, Dandan;
Jia, Xiaoyun;
Zhang, A-Mei;
Guo, Xiangming;
Zhang, Ya-Ping;
Zhang, Qingjiong;
Yao, Yong-Gang

Publication type:

Article

L239F founder mutation in GDAP1 is associated with a mild Charcot–Marie–Tooth type 4C4 (CMT4C4) phenotype.

Published in:

Neurogenetics, 2010, v. 11, n. 3, p. 357, doi. 10.1007/s10048-010-0237-6

By:

Kabzińska, Dagmara;
Strugalska-Cynowska, Halina;
Kostera-Pruszczyk, Anna;
Ryniewicz, Barbara;
Posmyk, Renata;
Midro, Alina;
Seeman, Pavel;
Báranková, Lucia;
Zimoń, Magdalena;
Baets, Jonathan;
Timmerman, Vincent;
Guergueltcheva, Velina;
Tournev, Ivailo;
Sarafov, Stayko;
Jonghe, Peter;
Jordanova, Albena;
Hausmanowa-Petrusewicz, Irena;
Kochański, Andrzej

Publication type:

Article

Questionable association between a monoamine oxidase A promoter polymorphism and sudden infant death syndrome.

Published in:

2010

By:

Klintschar, Michael;
Heimbold, Christian

Publication type:

Letter

Meta-analysis of association between variation in the PDE4D gene and ischemic cerebral infarction risk in Asian populations.

Published in:

Neurogenetics, 2010, v. 11, n. 3, p. 327, doi. 10.1007/s10048-010-0235-8

By:

Xu, Xiaowei;
Li, Xia;
Li, Jiejie;
Ou, Ru;
Sheng, Wenli

Publication type:

Article

Fine mapping of the chromosome 10q11-q21 linkage region in Alzheimer's disease cases and controls.

Published in:

Neurogenetics, 2010, v. 11, n. 3, p. 335, doi. 10.1007/s10048-010-0234-9

By:

Fallin, Margaret;
Szymanski, Megan;
Wang, Ruihua;
Gherman, Adrian;
Bassett, Susan;
Avramopoulos, Dimitrios

Publication type:

Article