Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland

被引：0

作者：

Auranen, M

Varilo, T

Alen, R

Vanhala, R

Ayers, K

Kempas, E

Ylisaukko-oja, T

Sinsheimer, JS

Peltonen, L

Järvelä, I

机构：

[1] Natl Publ Hlth Inst, Dept Mol Med, Helsinki, Finland

[2] Univ Helsinki, Dept Med Genet, FIN-00014 Helsinki, Finland

[3] Kuopio Univ Hosp, Unit Child Neurol, SF-70210 Kuopio, Finland

[4] Hosp Children & Adolescents, Unit Child Neurol, Helsinki, Finland

[5] Univ Calif Los Angeles, Sch Med, Dept Biomath, Los Angeles, CA 90024 USA

[6] Univ Calif Los Angeles, Sch Med, Dept Human Genet, Los Angeles, CA USA

[7] Univ Helsinki, Genet Mol Lab, Cent Hosp, FIN-00014 Helsinki, Finland

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 2002年 / 114卷 / 07期

关键词：

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

O43

引用

页码：728 / 728

页数：1

共 14 条

[1] Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland
Auranen, M
Varilo, T
Alen, R
Vanhala, R
Ayers, K
Kempas, E
Ylisaukko-oja, T
Peltonen, L
Järvelä, I
MOLECULAR PSYCHIATRY, 2003, 8 (10) : 879 - 884
[2] Evidence for allelic association on chromosome 3q25–27 in families with autism spectrum disorders originating from a subisolate of Finland
M Auranen
T Varilo
R Alen
R Vanhala
K Ayers
E Kempas
T Ylisaukko-oja
L Peltonen
I Järvelä
Molecular Psychiatry, 2003, 8 : 879 - 884
[3] A genomewide screen for autism-spectrum disorders:: Evidence for a major susceptibility locus on chromosome 3q25-27
Auranen, M
Vanhala, R
Varilo, T
Ayers, K
Kempas, E
Ylisaukko-oja, T
Sinsheimer, JS
Peltonen, L
Järvelä, I
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 777 - 790
[4] A major susceptibility locus for autism spectrum disorders on chromosome 3q25-27 in the Finnish population.
Auranen, MP
Kempas, E
Vanhala, R
Varilo, T
Ylisaukko-oja, T
Peltonen, L
Järvelä, I
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 200 - 200
[5] Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigree
Coon, H
Matsunami, N
Stevens, J
Miller, J
Pingree, C
Camp, NJ
Thomas, A
Krasny, L
Lainhart, J
Leppert, MF
McMahon, W
HUMAN HEREDITY, 2005, 60 (04) : 220 - 226
[6] Pharmacotherapeutic Implications of the Association Between Genomic Instability at Chromosome 15q13.3 and Autism Spectrum Disorders
Deutsch, Stephen I.
Urbano, Maria R.
Burket, Jessica A.
Herndon, Amy L.
Winebarger, Erin E.
CLINICAL NEUROPHARMACOLOGY, 2011, 34 (06) : 203 - 205
[7] Association analysis of SLC25A12 and EN2 in the Finnish families with autism-spectrum disorders
Turunen, Joni
Ylisaukko-oja, Tero
Kilpinen, Helena
Rehnstrom, Karola
Kempas, Elli
Vanhala, Raija
Wendt, Taina Nieminen-von
von Wendt, Lennart
Peltonen, Leena
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2006, 141B (07) : 766 - 766
[8] Clinical significance of association of allelic loss of chromosome 3P25 with alterations of chromosome 5Q22.3-Q23.2 in conventional renal cell carcinoma
Nagao, K
Yamaguchi, S
Yoshihiro, S
Matsuyama, H
Oba, K
Naito, K
JOURNAL OF UROLOGY, 2004, 171 (04): : 203 - 203
[9] An association analysis of GABRB3, a candidate gene of the GABAA receptor complex on chromosome 15Q and autism spectrum disorder
Curran, SR
Powell, J
Neale, BM
Dworzynski, K
Li, T
Thomas, S
Brown, J
Veltman, M
Rioberts, S
Murphy, D
Sham, P
Bolton, P
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2005, 138B (01) : 66 - 66
[10] Further evidence for a bipolar risk gene on chromosome 12q24 suggested by investigation of haplotype sharing and allelic association in patients from the Faroe Islands
Degn, B
Lundorf, MD
Wang, AG
Vang, M
Mors, O
Kruse, TA
Ewald, H
AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 105 (07): : 590 - 590

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