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Results: 1-25 | 26-38
Results: 1-25/38
HYDROCEPHALUS AND SPASTIC PARAPLEGIA RESULT FROM A DONOR SPLICE-SITE MUTATION (2872+1G TO 2872+1A) IN THE L1CAM GENE IN A VENEZUELAN PEDIGREE
Authors: CLAES S AGUIRRE T SIMOSA V LANDER R PIRAS M LEGIUS E CASSIMAN JJ RAEYMAEKERS P
Citation: S. Claes et al., HYDROCEPHALUS AND SPASTIC PARAPLEGIA RESULT FROM A DONOR SPLICE-SITE MUTATION (2872+1G TO 2872+1A) IN THE L1CAM GENE IN A VENEZUELAN PEDIGREE, Human mutation, 1998, pp. 240-241
REGION-SPECIFIC ISOLATION AND CHARACTERIZATION OF TRIPLET REPEATS
Authors: GOOSSENS D HARDING B RAEYMAEKERS P VANBROECKHOVEN C DELFAVERO J
Citation: D. Goossens et al., REGION-SPECIFIC ISOLATION AND CHARACTERIZATION OF TRIPLET REPEATS, American journal of medical genetics, 81(6), 1998, pp. 468-469
MANIC-DEPRESSIVE DISORDER AND CHROMOSOME-18
Authors: VILLAFUERTE SM VERHEYEN GR DELFAVERO J SOUERY D MENDLEWICZ J RAEYMAEKERS P VANBROECKHOVEN C
Citation: Sm. Villafuerte et al., MANIC-DEPRESSIVE DISORDER AND CHROMOSOME-18, American journal of medical genetics, 81(6), 1998, pp. 475-476
THE USE OF EXTREMELY HIGH AND LOW SCORING INDIVIDUALS ON TEMPERAMENT SCALES IN GENETIC ANALYSES - A POWER CALCULATION
Authors: VANGESTEL S FORSGREN T VERHEYEN G LUNDBERG M NILSSON LG VANBROECKHOVEN C RAEYMAEKERS P ADOLFSSON R
Citation: S. Vangestel et al., THE USE OF EXTREMELY HIGH AND LOW SCORING INDIVIDUALS ON TEMPERAMENT SCALES IN GENETIC ANALYSES - A POWER CALCULATION, American journal of medical genetics, 81(6), 1998, pp. 487-487
A EUROPEAN MULTICENTER ASSOCIATION STUDY WITH 5-HT2A RECEPTOR POLYMORPHISM IN UNIPOLAR AND BIPOLAR AFFECTIVE-DISORDERS
Authors: MASSAT I SOUERY D LIPP O MAHIEU B VERHEYEN G RAEYMAEKERS P SERRETTI A MACCIARDI F VANBROECKHOVEN C MENDLEWICZ J
Citation: I. Massat et al., A EUROPEAN MULTICENTER ASSOCIATION STUDY WITH 5-HT2A RECEPTOR POLYMORPHISM IN UNIPOLAR AND BIPOLAR AFFECTIVE-DISORDERS, American journal of medical genetics, 81(6), 1998, pp. 502-502
TYROSINE-HYDROXYLASE POLYMORPHISM AND PHENOTYPIC HETEROGENEITY IN UNIPOLAR AFFECTIVE-DISORDER - A EUROPEAN MULTICENTER ASSOCIATION STUDY
Authors: SOUERY D LIPP O RIVELLI S CAVALLINI C RAEYMAEKERS P VERHEYEN G MACCIARDI F VANBROECKHOVEN C MENDLEWICZ J
Citation: D. Souery et al., TYROSINE-HYDROXYLASE POLYMORPHISM AND PHENOTYPIC HETEROGENEITY IN UNIPOLAR AFFECTIVE-DISORDER - A EUROPEAN MULTICENTER ASSOCIATION STUDY, American journal of medical genetics, 81(6), 1998, pp. 511-511
ASSOCIATION BETWEEN SOCIAL-ADJUSTMENT AND CANDIDATE GENES POLYMORPHISM IN REMITTED BIPOLAR AND UNIPOLAR PATIENTS
Authors: BLAIRY S SOUERY D LIPP O VERHEYEN G RAEYMAEKERS P SERRETTI A MACCIARDI F VANBROECKHOVEN C MENDLEWICZ J
Citation: S. Blairy et al., ASSOCIATION BETWEEN SOCIAL-ADJUSTMENT AND CANDIDATE GENES POLYMORPHISM IN REMITTED BIPOLAR AND UNIPOLAR PATIENTS, American journal of medical genetics, 81(6), 1998, pp. 522-522
GENETIC-ANALYSIS OF THE 12Q CANDIDATE REGION FOR BIPOLAR DISORDER
Authors: VERHEYEN GR ORUC L SOUERY D CLAES S AALBREGTSE M CASSIMAN JJ MENDLEWICZ J IVEZIC S VANBROECKHOVEN C RAEYMAEKERS P
Citation: Gr. Verheyen et al., GENETIC-ANALYSIS OF THE 12Q CANDIDATE REGION FOR BIPOLAR DISORDER, American journal of medical genetics, 81(6), 1998, pp. 540-541
THE X-LINKED INFANTILE SPASMS SYNDROME (MIM-308350) MAPS TO XP11.4-XPTER IN 2 PEDIGREES
Authors: CLAES S DEVRIENDT K LAGAE L CEULEMANS B DOM L CASAER P RAEYMAEKERS P CASSIMAN JJ FRYNS JP
Citation: S. Claes et al., THE X-LINKED INFANTILE SPASMS SYNDROME (MIM-308350) MAPS TO XP11.4-XPTER IN 2 PEDIGREES, Annals of neurology, 42(3), 1997, pp. 360-364
POSITIVE ASSOCIATION BETWEEN THE GABRA5 GENE AND UNIPOLAR RECURRENT MAJOR DEPRESSION
Authors: ORUC L VERHEYEN GR FURAC I IVEZIC S JAKOVLJEVIC M RAEYMAEKERS P VANBROECKHOVEN C
Citation: L. Oruc et al., POSITIVE ASSOCIATION BETWEEN THE GABRA5 GENE AND UNIPOLAR RECURRENT MAJOR DEPRESSION, Neuropsychobiology, 36(2), 1997, pp. 62-64
A CHROMOSOME-18 GENETIC-LINKAGE STUDY IN 3 LARGE BELGIAN PEDIGREES WITH BIPOLAR DISORDER
Authors: CLAES S RAEYMAEKERS P VANDENBROECK M DIEPENDAELE S DEBRUYN A VERHEYEN G WILS V BOOGAERTS A TANGHE A GODDERIS J VANBROECKHOVEN C CASSIMAN JJ
Citation: S. Claes et al., A CHROMOSOME-18 GENETIC-LINKAGE STUDY IN 3 LARGE BELGIAN PEDIGREES WITH BIPOLAR DISORDER, Journal of affective disorders, 43(3), 1997, pp. 195-205
LINKAGE STUDIES WITH CHROMOSOMAL CANDIDATE REGIONS IN BIPOLAR FAMILIES
Authors: RAEYMAEKERS P VERHEYEN GR VANZAND K SOUERY D CLAES S GODDERIS J CASSIMAN JJ MENDLEWICZ J VANBROECKHOVEN C
Citation: P. Raeymaekers et al., LINKAGE STUDIES WITH CHROMOSOMAL CANDIDATE REGIONS IN BIPOLAR FAMILIES, American journal of medical genetics, 74(6), 1997, pp. 587-587
GENETIC AND PHYSICAL MAPPING OF THE CHROMOSOME 18Q22.1-Q22.3 CANDIDATE REGION FOR BIPOLAR DISORDER
Authors: VERHEYEN GR VILLAFUERTE S RAEYMAEKERS P DELFAVERO J SOUERY D MENDLEWICZ J VANBROECKHOVEN C
Citation: Gr. Verheyen et al., GENETIC AND PHYSICAL MAPPING OF THE CHROMOSOME 18Q22.1-Q22.3 CANDIDATE REGION FOR BIPOLAR DISORDER, American journal of medical genetics, 74(6), 1997, pp. 676-676
THE X-LINKED INFANTILE-SPASMS-SYNDROME (MIM-308350) MAPS TO XP11.4-XPTER IN 2 PEDIGREES
Authors: CLAES S DEVRIENDT K LAGAE L RAEYMAEKERS P CASSIMAN JJ FRYNS JP
Citation: S. Claes et al., THE X-LINKED INFANTILE-SPASMS-SYNDROME (MIM-308350) MAPS TO XP11.4-XPTER IN 2 PEDIGREES, American journal of medical genetics, 74(6), 1997, pp. 678-679
ASSOCIATION ANALYSIS OF THE 5-HT2C RECEPTOR AND 5-HT TRANSPORTER GENES IN BIPOLAR DISORDER
Authors: ORUC L VERHEYEN GR FURAC I JAKOVLJEVIC M IVEZIC S RAEYMAEKERS P VANBROECKHOVEN C
Citation: L. Oruc et al., ASSOCIATION ANALYSIS OF THE 5-HT2C RECEPTOR AND 5-HT TRANSPORTER GENES IN BIPOLAR DISORDER, American journal of medical genetics, 74(5), 1997, pp. 504-506
ANALYSIS OF THE TYROSINE-HYDROXYLASE AND DOPAMINE D4 RECEPTOR GENES IN A CROATIAN SAMPLE OF BIPOLAR-I AND UNIPOLAR PATIENTS
Authors: ORUC L VERHEYEN GR FURAC I JAKOVLJEVIC M IVEZIC S RAEYMAEKERS P VANBROECKHOVEN C
Citation: L. Oruc et al., ANALYSIS OF THE TYROSINE-HYDROXYLASE AND DOPAMINE D4 RECEPTOR GENES IN A CROATIAN SAMPLE OF BIPOLAR-I AND UNIPOLAR PATIENTS, American journal of medical genetics, 74(2), 1997, pp. 176-178
REGIONAL LOCALIZATION OF 2 GENES FOR NONSPECIFIC X-LINKED MENTAL-RETARDATION TO XP22.3-P22.2 (MRX49) AND XP11.3-P11.21 (MRX50)
Authors: CLAES S VOGELS A HOLVOET M DEVRIENDT K RAEYMAEKERS P CASSIMAN JJ FRYNS JP
Citation: S. Claes et al., REGIONAL LOCALIZATION OF 2 GENES FOR NONSPECIFIC X-LINKED MENTAL-RETARDATION TO XP22.3-P22.2 (MRX49) AND XP11.3-P11.21 (MRX50), American journal of medical genetics, 73(4), 1997, pp. 474-479
X-LINKED SEVERE MENTAL-RETARDATION AND A PROGRESSIVE NEUROLOGICAL DISORDER IN A BELGIAN FAMILY - CLINICAL AND GENETIC-STUDIES
Authors: CLAES S DEVRIENDT K DADAMO P MEIRELEIRE J RAEYMAEKERS P TONIOLO D CASSIMAN JJ FRYNS JP
Citation: S. Claes et al., X-LINKED SEVERE MENTAL-RETARDATION AND A PROGRESSIVE NEUROLOGICAL DISORDER IN A BELGIAN FAMILY - CLINICAL AND GENETIC-STUDIES, Clinical genetics, 52(3), 1997, pp. 155-161
CAG REPEAT EXPANSIONS IN BIPOLAR AND UNIPOLAR DISORDERS
Authors: ORUC L LINDBLAD K VERHEYEN GR AHLBERG S JAKOVLJEVIC M IVEZIC S RAEYMAEKERS P VANBROECKHOVEN C SCHALLING M
Citation: L. Oruc et al., CAG REPEAT EXPANSIONS IN BIPOLAR AND UNIPOLAR DISORDERS, American journal of human genetics, 60(3), 1997, pp. 730-732
IDENTIFICATION OF A NEW LOCUS FOR AUTOSOMAL-DOMINANT NON-SYNDROMIC HEARING IMPAIRMENT (DFNA7) IN A LARGE NORWEGIAN FAMILY
Authors: FAGERHEIM T NILSSEN O RAEYMAEKERS P BROX V MOUM T ELVERLAND HH TEIG E OMLAND HH FOSTAD GK TRANEBJAERG L
Citation: T. Fagerheim et al., IDENTIFICATION OF A NEW LOCUS FOR AUTOSOMAL-DOMINANT NON-SYNDROMIC HEARING IMPAIRMENT (DFNA7) IN A LARGE NORWEGIAN FAMILY, Human molecular genetics, 5(8), 1996, pp. 1187-1191
LINKAGE OF TYPE-I DIABETES TO 15Q26 (IDDM3) IN THE DANISH POPULATION
Authors: ZAMANI M POCIOT F RAEYMAEKERS P NERUP J CASSIMAN JJ
Citation: M. Zamani et al., LINKAGE OF TYPE-I DIABETES TO 15Q26 (IDDM3) IN THE DANISH POPULATION, Human genetics, 98(4), 1996, pp. 491-496
A FORM OF NONSPECIFIC MENTAL-RETARDATION IS PROBABLY CAUSED BY A MICRODELETION IN A BELGIAN FAMILY
Authors: RAEYMAEKERS P LIN J GU XX SOEKARMAN D CASSIMAN JJ FRYNS JP MARYNEN P
Citation: P. Raeymaekers et al., A FORM OF NONSPECIFIC MENTAL-RETARDATION IS PROBABLY CAUSED BY A MICRODELETION IN A BELGIAN FAMILY, American journal of medical genetics, 64(1), 1996, pp. 16-16
LINKAGE ANALYSIS IN 3 FAMILIES WITH NONSPECIFIC X-LINKED MENTAL-RETARDATION
Authors: CLAES S GU XX LEGIUS E LORENZETTI E MARYNEN P FRYNS JP CASSIMAN JJ RAEYMAEKERS P
Citation: S. Claes et al., LINKAGE ANALYSIS IN 3 FAMILIES WITH NONSPECIFIC X-LINKED MENTAL-RETARDATION, American journal of medical genetics, 64(1), 1996, pp. 137-146
LINKAGE AND ASSOCIATION OF THE HLA GENE-COMPLEX WITH IDDM IN 81 DANISH FAMILIES - STRONG LINKAGE BETWEEN DR-BETA-1(LYS71+) AND IDDM
Authors: ZAMANI M POCIOT F SPAEPEN M RAEYMAEKERS P NERUP J CASSIMAN JJ
Citation: M. Zamani et al., LINKAGE AND ASSOCIATION OF THE HLA GENE-COMPLEX WITH IDDM IN 81 DANISH FAMILIES - STRONG LINKAGE BETWEEN DR-BETA-1(LYS71+) AND IDDM, Journal of Medical Genetics, 33(11), 1996, pp. 899-905
LOCALIZATION OF A NEW GENE FOR NONSPECIFIC MENTAL-RETARDATION TO XQ22-Q26 (MRX35)
Authors: GU XX DECORTE R MARYNEN P FRYNS JP CASSIMAN JJ RAEYMAEKERS P
Citation: Xx. Gu et al., LOCALIZATION OF A NEW GENE FOR NONSPECIFIC MENTAL-RETARDATION TO XQ22-Q26 (MRX35), Journal of Medical Genetics, 33(1), 1996, pp. 52-55
Risultati: 1-25 | 26-38