Nonreplication of linkage disequilibrium between the dopamine D4 receptor locus and Tourette syndrome

被引：29

作者：

Hebebrand, J

Nothen, MM

Ziegler, A

Klug, B

Neidt, H

Eggermann, K

Lehmkuhl, G

Poustka, F

Schmidt, MH

Propping, P

Remschmidt, H

机构：

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1997年 / 61卷 / 01期

关键词：

D O I：

10.1016/S0002-9297(07)64298-0

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：238 / 239

页数：2

共 9 条

[1] DISTRIBUTION OF A NOVEL MUTATION IN THE 1ST EXON OF THE HUMAN DOPAMINE-D(4) RECEPTOR GENE IN PSYCHOTIC-PATIENTS [J].

CATALANO, M ;

NOBILE, M ;

NOVELLI, E ;

NOTHEN, MM ;

SMERALDI, E .

BIOLOGICAL PSYCHIATRY, 1993, 34 (07) :459-464

[2] Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor gene [J].

Cichon, S ;

Nothen, MM ;

Catalano, M ;

DiBella, D ;

Maier, W ;

Lichtermann, D ;

Minges, J ;

Albus, M ;

Borrmann, M ;

Franzek, E ;

Stober, G ;

Weigelt, B ;

Korner, J ;

Rietschel, M ;

Propping, P .

PSYCHIATRIC GENETICS, 1995, 5 (03) :97-103

[3]

Grice DE, 1996, AM J HUM GENET, V59, P644

[4] TOURETTES-SYNDROME AND HOMOZYGOSITY FOR THE DOPAMINE-D3 RECEPTOR GENE [J].

HEBEBRAND, J ;

NOTHEN, MM ;

LEHMKUHL, G ;

POUSTKA, F ;

SCHMIDT, M ;

PROPPING, P ;

REMSCHMIDT, H .

LANCET, 1993, 341 (8858) :1483-1483

[5] A HYPERVARIABLE SEGMENT IN THE HUMAN DOPAMINE RECEPTOR D(4) (DRD4) GENE [J].

LICHTER, JB ;

BARR, CL ;

KENNEDY, JL ;

VANTOL, HHM ;

KIDD, KK ;

LIVAK, KJ .

HUMAN MOLECULAR GENETICS, 1993, 2 (06) :767-773

[6] HUMAN DOPAMINE D4 RECEPTOR GENE - FREQUENT OCCURRENCE OF A NULL ALLELE AND OBSERVATION OF HOMOZYGOSITY [J].

NOTHEN, MM ;

CICHON, S ;

HEMMER, S ;

HEBEBRAND, J ;

REMSCHMIDT, H ;

LEHMKUHL, G ;

POUSTKA, F ;

SCHMIDT, M ;

CATALANO, M ;

FIMMERS, R ;

KORNER, J ;

RIETSCHEL, M ;

PROPPING, P .

HUMAN MOLECULAR GENETICS, 1994, 3 (12) :2207-2212

[7] ASSOCIATION ANALYSIS OF THE DOPAMINE D-2 RECEPTOR GENE IN TOURETTES-SYNDROME USING THE HAPLOTYPE RELATIVE RISK METHOD [J].

NOTHEN, MM ;

HEBEBRAND, J ;

KNAPP, M ;

HEBEBRAND, K ;

CAMPS, A ;

VONGONTARD, A ;

WETTKESCHAFER, R ;

LISCH, S ;

CICHON, S ;

POUSTKA, F ;

SCHMIDT, M ;

LEHMKUHL, G ;

REMSCHMIDT, H ;

PROPPING, P .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 54 (03) :249-252

[8]

SPIELMAN RS, 1993, AM J HUM GENET, V52, P506

[9]

VANTOL HHM, 1992, NATURE, V358, P149

← 1 →