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Results: 26-50/56
Authors:
MOWRY BJ
NANCARROW DJ
LENNON DP
SANDKUIJL LA
CROWE RR
SILVERMAN JM
MOHS RC
SIEVER LJ
ENDICOTT J
SHARPE L
WALTERS MK
HAYWARD NK
LEVINSON DF
Citation: Bj. Mowry et al., SCHIZOPHRENIA SUSCEPTIBILITY AND CHROMOSOME 6P24-22, Nature genetics, 11(3), 1995, pp. 233-234
Authors:
GRUIS NA
VANDERVELDEN PA
SANDKUIJL LA
PRINS DE
WEAVERFELDHAUS J
KAMB A
BERGMAN W
FRANTS RR
Citation: Na. Gruis et al., HOMOZYGOTES FOR CDKN2 (P16) GERMLINE MUTATION IN DUTCH FAMILIAL MELANOMA KINDREDS, Nature genetics, 10(3), 1995, pp. 351-353
Authors:
GRUIS NA
SANDKUIJL LA
VANDERVELDEN PA
BERGMAN W
FRANTS RR
Citation: Na. Gruis et al., CDKN2 EXPLAINS PART OF THE CLINICAL PHENOTYPE IN DUTCH FAMILIAL ATYPICAL MULTIPLE-MOLE MELANOMA (FAMMM) SYNDROME FAMILIES, Melanoma research, 5(3), 1995, pp. 169-177
Authors:
TEMEERMAN GJ
VANDERMEULEN MA
SANDKUIJL LA
Citation: Gj. Temeerman et al., PERSPECTIVES OF IDENTITY BY DESCENT (IBD) MAPPING IN FOUNDER POPULATIONS, Clinical and experimental allergy, 25, 1995, pp. 97-102
Authors:
HOUWINGDUISTERMAAT JJ
SANDKUIJL LA
BERGEN AAB
VANHOUWELINGEN HC
Citation: Jj. Houwingduistermaat et al., MAXIMUM-LIKELIHOOD-ESTIMATION IN LINKAGE HETEROGENEITY MODELS INCLUDING ADDITIONAL INFORMATION VIA THE EM ALGORITHM, Genetic epidemiology, 12(5), 1995, pp. 515-527
Authors:
MAY A
OPHOFF RA
TERWINDT GM
URBAN C
VANEIJK R
HAAN J
DIENER HC
LINDHOUT D
FRANTS RR
SANDKUIJL LA
FERRARI MD
Citation: A. May et al., FAMILIAL HEMIPLEGIC MIGRAINE LOCUS ON 19P13 IS INVOLVED IN THE COMMONFORMS OF MIGRAINE WITH AND WITHOUT AURA, Human genetics, 96(5), 1995, pp. 604-608
Authors:
DEKONING TJ
SANDKUIJL LA
DESCHRYVER JEAR
HENNEKAM EAM
BEEMER FA
HOUWEN RHJ
Citation: Tj. Dekoning et al., AUTOSOMAL-RECESSIVE INHERITANCE OF BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS, American journal of medical genetics, 57(3), 1995, pp. 479-482
Authors:
PADBERG GW
FRANTS RR
BROUWER OF
WIJMENGA C
BAKKER E
SANDKUIJL LA
Citation: Gw. Padberg et al., FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY IN THE DUTCH POPULATION, Muscle & nerve, 1995, pp. 81-84
Authors:
BOERMAN RH
OPHOFF RA
LINKS TP
VANEIJK R
SANDKUIJL LA
ELBAZ A
VALESANTOS JE
WINTZEN AR
VANDEUTEKOM JC
ISLES DE
FONTAINE B
PADBERG GW
FRANTS RR
Citation: Rh. Boerman et al., MUTATION IN DHP RECEPTOR ALPHA-1 SUBUNIT (CACLN1A3) GENE IN A DUTCH FAMILY WITH HYPOKALEMIC PERIODIC PARALYSIS, Journal of Medical Genetics, 32(1), 1995, pp. 44-47
Authors:
GRUIS NA
VANDERVELDEN PA
SANDKUIJL LA
PRINS DE
BERGMAN W
FRANTS RR
VERMEER BJ
Citation: Na. Gruis et al., HOMOZYGOTES FOR CDKN2 P16 GERMLINE MUTATION IN DUTCH FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA (FAMMM) SYNDROME FAMILIES ARE VIABLE/, Journal of investigative dermatology, 104(4), 1995, pp. 584-584
Authors:
TIJSSEN MAJ
SHIANG R
VANDEUTEKOM J
BOERMAN RH
WASMUTH JJ
SANDKUIJL LA
FRANTS RR
PADBERG GW
Citation: Maj. Tijssen et al., MOLECULAR-GENETIC REEVALUATION OF THE DUTCH HYPEREKPLEXIA FAMILY, Archives of neurology, 52(6), 1995, pp. 578-582
Authors:
FRANTS RR
VANDERVELDEN PA
SANDKUIJL LA
PRINS DE
BERGMAN W
GRUIS NA
Citation: Rr. Frants et al., VIABILITY OF HOMOZYGOTES FOR A GERMLINE DELETION OF 19 BP IN THE CODING REGION OF THE CDKN2 P16 GENE IN DUTCH MELANOMA FAMILIES/, American journal of human genetics, 57(4), 1995, pp. 338-338
Authors:
HEUTINK P
VANDEWETERING BJM
PAKSTIS AJ
KURLAN R
SANDOR P
OOSTRA BA
SANDKUIJL LA
Citation: P. Heutink et al., LINKAGE STUDIES ON GILLES-DE-LA-TOURETTE SYNDROME - WHAT IS THE STRATEGY OF CHOICE, American journal of human genetics, 57(2), 1995, pp. 465-473
Authors:
MITCHISON HM
ORAWE AM
TASCHNER PEM
SANDKUIJL LA
SANTAVUORI P
DEVOS N
BREUNING MH
MOLE SE
GARDINER RM
JARVELA IE
Citation: Hm. Mitchison et al., BATTEN-DISEASE GENE, CLN3 - LINKAGE DISEQUILIBRIUM MAPPING IN THE FINNISH POPULATION, AND ANALYSIS OF EUROPEAN HAPLOTYPES, American journal of human genetics, 56(3), 1995, pp. 654-662
Authors:
HOUWEN RHJ
BAHARLOO S
BLANKENSHIP K
RAEYMAEKERS P
JUYN J
SANDKUIJL LA
FREIMER NB
Citation: Rhj. Houwen et al., GENOME SCREENING BY SEARCHING FOR SHARED SEGMENTS - MAPPING A GENE FOR BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS, Nature genetics, 8(4), 1994, pp. 380-386
Authors:
HEUTINK P
ZGURICAS J
VANOOSTERHOUT L
BREEDVELD GJ
TESTERS L
SANDKUIJL LA
SNIJDERS PJLM
WEISSENBACH J
LINDHOUT D
HOVIUS SER
OOSTRA BA
Citation: P. Heutink et al., THE GENE FOR TRIPHALANGEAL THUMB MAPS TO THE SUBTELOMERIC REGION OF CHROMOSOME 7Q, Nature genetics, 6(3), 1994, pp. 287-292
Authors:
WU YQ
HEUTINK P
DEVRIES BBA
SANDKUIJL LA
VANDENOUWELAND AMW
NIERMEIJER MF
GALJAARD H
REYNIERS E
WILLEMS PJ
HALLEY DJJ
Citation: Yq. Wu et al., ASSIGNMENT OF A 2ND LOCUS FOR MULTIPLE EXOSTOSES TO THE PERICENTROMERIC REGION OF CHROMOSOME-11, Human molecular genetics, 3(1), 1994, pp. 167-171
Authors:
VANSOEST S
VANDENBORN LI
GAL A
FARRAR GJ
BLEEKERWAGEMAKERS LM
WESTERVELD A
HUMPHRIES P
SANDKUIJL LA
BERGEN AAB
Citation: S. Vansoest et al., ASSIGNMENT OF A GENE FOR AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA (RP12) TO CHROMOSOME 1Q31-Q32.1 IN AN INBRED AND GENETICALLY HETEROGENEOUS DISEASE POPULATION, Genomics, 22(3), 1994, pp. 499-504
Authors:
OPHOFF RA
VANEIJK R
SANDKUIJL LA
TERWINDT GM
GRUBBEN CPM
HAAN J
LINDHOUT D
FERRARI MD
FRANTS RR
Citation: Ra. Ophoff et al., GENETIC-HETEROGENEITY OF FAMILIAL HEMIPLEGIC MIGRAINE, Genomics, 22(1), 1994, pp. 21-26
Authors:
VANDEUTEKOM JCT
BRUYN RPM
VANDENBOORN N
SANDKUIJL LA
PADBERG GW
FRANTS RR
Citation: Jct. Vandeutekom et al., PURE HEREDITARY SPASTIC PARAPARESIS - AN EXCLUSION MAP COVERING MORE THAN 40-PERCENT OF THE AUTOSOMAL GENOME, Human genetics, 93(4), 1994, pp. 408-414
Authors:
DEBRUYN A
RAEYMAEKERS P
MENDELBAUM K
SANDKUIJL LA
RAES G
DELVENNE V
HIRSCH D
STANER L
MENDLEWICZ J
VANBROECKHOVEN C
Citation: A. Debruyn et al., LINKAGE ANALYSIS OF BIPOLAR ILLNESS WITH X-CHROMOSOME DNA MARKERS - ASUSCEPTIBILITY GENE IN XQ27-Q28 CANNOT BE EXCLUDED, American journal of medical genetics, 54(4), 1994, pp. 411-419
Authors:
HEUTINK P
HAITJEMA T
BREEDVELD GJ
JANSSEN B
SANDKUIJL LA
BONTEKOE CJM
WESTERMAN CJJ
OOSTRA BA
Citation: P. Heutink et al., LINKAGE OF HEREDITARY HEMORRHAGIC TELANGIECTASIA TO CHROMOSOME 9Q34 AND EVIDENCE FOR LOCUS HETEROGENEITY, Journal of Medical Genetics, 31(12), 1994, pp. 933-936
Authors:
BERGMAN W
GRUIS NA
SANDKUIJL LA
FRANTS RR
Citation: W. Bergman et al., GENETICS OF 7 DUTCH FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA SYNDROMEFAMILIES - A REVIEW OF LINKAGE RESULTS INCLUDING CHROMOSOME-1 AND CHROMOSOME-9, Journal of investigative dermatology, 103(5), 1994, pp. 190000122-190000125
Authors:
DEBRUYN A
MENDELBAUM K
SANDKUIJL LA
DELVENNE V
HIRSCH D
STANER L
MENDLEWICZ J
VANBROECKHOVEN C
Citation: A. Debruyn et al., NONLINKAGE OF BIPOLAR ILLNESS TO TYROSINE-HYDROXYLASE, TYROSINASE, AND D-2 AND D-4 DOPAMINE-RECEPTOR GENES ON CHROMOSOME 11, The American journal of psychiatry, 151(1), 1994, pp. 102-106
Authors:
RANUM LPW
CHUNG MY
BANFI S
BRYER A
SCHUT LJ
RAMESAR R
DUVICK LA
MCCALL A
SUBRAMONY SH
GOLDFARB L
GOMEZ C
SANDKUIJL LA
ORR HT
ZOGHBI HY
Citation: Lpw. Ranum et al., MOLECULAR AND CLINICAL CORRELATIONS IN SPINOCEREBELLAR ATAXIA TYPE-I - EVIDENCE FOR FAMILIAL EFFECTS ON THE AGE AT ONSET, American journal of human genetics, 55(2), 1994, pp. 244-252