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Results: 1-9 |
Results: 9
AFFECTIVE SYMPTOMS AND FAMILY HISTORY OF AFFECTIVE-DISORDER IN PATIENTS WITH TARDIVE-DYSKINESIA
Authors: SCHULZE TG MAROLDT A KRAUSS H KNAPP M MARWINSKI K FERNANDEZ ANY MULLER DJ WEBER T NOTHEN M MAIER W HELD T RIETSCHEL M
Citation: Tg. Schulze et al., AFFECTIVE SYMPTOMS AND FAMILY HISTORY OF AFFECTIVE-DISORDER IN PATIENTS WITH TARDIVE-DYSKINESIA, American journal of medical genetics, 81(6), 1998, pp. 526-527
FAMILIAL OCCURRENCE OF TARDIVE-DYSKINESIA
Authors: MULLER DJ AHLE G ALFTER D KRAUSS H KNAPP M MARWINSKI K SCHULZE TG WEBER T NOTHEN M MAIER W HELD T RIETSCHEL M
Citation: Dj. Muller et al., FAMILIAL OCCURRENCE OF TARDIVE-DYSKINESIA, American journal of medical genetics, 81(6), 1998, pp. 527-527
METAANALYSIS OF ASSOCIATION STUDIES BETWEEN SCHIZOPHRENIA AND POLYMORPHISMS OF THE 5-HYDROXYTRYPTAMINE TYPE 2A RECEPTOR GENE
Authors: SPURLOCK G WILLIAMS J MCGUFFIN P MALLET J NOTHEN M GILL M ASCHAUER H ADOLFSSON R MACCIARDI F OWEN MJ
Citation: G. Spurlock et al., METAANALYSIS OF ASSOCIATION STUDIES BETWEEN SCHIZOPHRENIA AND POLYMORPHISMS OF THE 5-HYDROXYTRYPTAMINE TYPE 2A RECEPTOR GENE, Schizophrenia research, 24(1-2), 1997, pp. 91-91
DESCRIPTION OF THE GENETIC-ANALYSIS WORKSHOP-10 BIPOLAR DISORDER LINKAGE DATA SETS
Authors: GOLDIN LR GERSHON ES BERRETTINI WH STINE OC DEPAULO R MCMAHON F MEYERS D NOTHEN M PROPPING P CICHON S FIMMERS R BAUR M ALBUS M FRANZEK E KREINER R MAIER W RIETSCHEL M BARON M KNOWLES J GILLIAM C ENDICOTT J GURLING H CURTIS D SMYTH C KELSOE J
Citation: Lr. Goldin et al., DESCRIPTION OF THE GENETIC-ANALYSIS WORKSHOP-10 BIPOLAR DISORDER LINKAGE DATA SETS, Genetic epidemiology, 14(6), 1997, pp. 563-568
METAANALYSIS OF ASSOCIATION BETWEEN THE 5 HT2A RECEPTOR T102C POLYMORPHISM AND SCHIZOPHRENIA
Authors: WILLIAMS J MCGUFFIN P NOTHEN M OWEN MJ SPURLOCK G
Citation: J. Williams et al., METAANALYSIS OF ASSOCIATION BETWEEN THE 5 HT2A RECEPTOR T102C POLYMORPHISM AND SCHIZOPHRENIA, Lancet, 349(9060), 1997, pp. 1221-1221
LOCALIZATION OF THE HUMAN GLUCOSIDASE-I GENE TO CHROMOSOME-2P12-P13 BY FLUORESCENCE IN-SITU HYBRIDIZATION AND PCR ANALYSIS OF SOMATIC-CELL HYBRIDS
Authors: KALZFULLER B HEIDRICHKAUL C NOTHEN M BAUSE E SCHWANITZ G
Citation: B. Kalzfuller et al., LOCALIZATION OF THE HUMAN GLUCOSIDASE-I GENE TO CHROMOSOME-2P12-P13 BY FLUORESCENCE IN-SITU HYBRIDIZATION AND PCR ANALYSIS OF SOMATIC-CELL HYBRIDS, Genomics, 34(3), 1996, pp. 442-443
LINKAGE STUDIES OF BIPOLAR DISORDER IN THE REGION OF THE DARIERS-DISEASE GENE ON CHROMOSOME 12Q23-24.1
Authors: DAWSON E PARFITT E ROBERTS Q DANIELS J LIM L SHAM P NOTHEN M PROPPING P LANCZIK M MAIER W REUNER U WEISSENBACH J GILL M POWELL J MCGUFFIN P OWEN M CRADDOCK N
Citation: E. Dawson et al., LINKAGE STUDIES OF BIPOLAR DISORDER IN THE REGION OF THE DARIERS-DISEASE GENE ON CHROMOSOME 12Q23-24.1, American journal of medical genetics, 60(2), 1995, pp. 94-102
AN ASSOCIATION STUDY OF A NEUROTROPHIN-3 (NT-3) GENE POLYMORPHISM WITH SCHIZOPHRENIA
Authors: DAWSON E POWELL JF SHAM PC NOTHEN M CROCQ MA PROPPING P KORNER J RIETSCHEL M VANOS J WRIGHT P MURRAY RM GILL M
Citation: E. Dawson et al., AN ASSOCIATION STUDY OF A NEUROTROPHIN-3 (NT-3) GENE POLYMORPHISM WITH SCHIZOPHRENIA, Acta psychiatrica Scandinavica, 92(6), 1995, pp. 425-428
CLINICAL-EVIDENCE FOR GENOMIC IMPRINTING IN BIPOLAR-I DISORDER
Authors: GRIGOROIUSERBANESCU M NOTHEN M PROPPING P POUSTKA F MAGUREANU S VASILESCU R MARINESCU E ARDELEAN V
Citation: M. Grigoroiuserbanescu et al., CLINICAL-EVIDENCE FOR GENOMIC IMPRINTING IN BIPOLAR-I DISORDER, Acta psychiatrica Scandinavica, 92(5), 1995, pp. 365-370
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