GENETIC-LINKAGE IS EXCLUDED FOR THE D2-DOPAMINE RECEPTOR LAMBDA-HD2G1 AND FLANKING LOCI ON CHROMOSOME 11Q22-Q23 IN TOURETTE SYNDROME

被引：36

作者：

DEVOR, EJ

GRANDY, DK

CIVELLI, O

LITT, M

BURGESS, AK

ISENBERG, KE

VANDEWETERING, BJM

OOSTRA, B

机构：

[1] OREGON HLTH SCI UNIV,VOLLUM INST ADV BIOMED RES,PORTLAND,OR 97201

[2] OREGON HLTH SCI UNIV,DEPT MED GENET & BIOCHEM,PORTLAND,OR 97201

[3] ERASMUS UNIV,DEPT CLIN GENET,3000 DR ROTTERDAM,NETHERLANDS

来源：

HUMAN HEREDITY | 1990年 / 40卷 / 02期

关键词：

Chromosome; 11q; Linkage; Tourette syndrome;

D O I：

10.1159/000153914

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

A genetic linkage study of fifteen families (n = 166) ascertained through probands diagnosed for Tourette syndrome was carried out for the D2dopamine receptor and flanking loci on chromosome 11q22-q23. Tight linkage was excluded for all probes and regions of exclusion up to ±20% recombination were obtained. Overlapping regions of exclusion based upon primary map data permit exclusion of the entire region of the DRD2 locus in Tourette syndrome. © 1990 S. Karger AG, Basel.

引用

页码：105 / 108

页数：4

共 17 条

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