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Results: 76-100/339
THE GENE FOR X-LINKED HYPOPHOSPHATEMIC RICKETS MAPS TO A 200-300 KB REGION IN XP22.1, AND IS LOCATED ON A SINGLE YAC CONTAINING A PUTATIVE VITAMIN-D RESPONSE ELEMENT (VDRE)
Authors: ROWE PSN GOULDING JN FRANCIS F OUDET C ECONS MJ HANAUER A LEHRACH H READ AP MOUNTFORD RC SUMMERFIELD T WEISSENBACH J FRASER W DREZNER MK DAVIES KE ORIORDAN JLH
Citation: Psn. Rowe et al., THE GENE FOR X-LINKED HYPOPHOSPHATEMIC RICKETS MAPS TO A 200-300 KB REGION IN XP22.1, AND IS LOCATED ON A SINGLE YAC CONTAINING A PUTATIVE VITAMIN-D RESPONSE ELEMENT (VDRE), Human genetics, 97(3), 1996, pp. 345-352
LOCALIZATION OF THE FANCONI-ANEMIA COMPLEMENTATION GROUP-A GENE TO CHROMOSOME 16Q24.3
Authors: GIBSON RA PRONK JC SAVOIA A MORGAN NV WIJKER M HASSOCK S VETRIE D OLAVESEN M KENDALL E FAURE S WEISSENBACH J DOGGETT NA JOENJE H ARWERT F MATHEW CG
Citation: Ra. Gibson et al., LOCALIZATION OF THE FANCONI-ANEMIA COMPLEMENTATION GROUP-A GENE TO CHROMOSOME 16Q24.3, Cytogenetics and cell genetics, 72(4), 1996, pp. 11-11
A LOCUS FOR FANCONI-ANEMIA ON 16Q DETERMINED BY HOMOZYGOSITY MAPPING
Authors: GSCHWEND M LEVRAN O KRUGLYAK L RANDADE K VERLANDER PC SHEN S FAURE S WEISSENBACH J ALTAY C LANDER ES AUERBACH AD BOTSTEIN D
Citation: M. Gschwend et al., A LOCUS FOR FANCONI-ANEMIA ON 16Q DETERMINED BY HOMOZYGOSITY MAPPING, Cytogenetics and cell genetics, 72(4), 1996, pp. 13-13
IDENTIFICATION AND CLONING IN YEAST ARTIFICIAL CHROMOSOMES OF A REGION OF ELEVATED LOSS OF HETEROZYGOSITY ON CHROMOSOME 1P31.1
Authors: HEY Y HOGGARD N BRINTNELL B JAMES L JONES D MITCHELL E WEISSENBACH J VARLEY JM
Citation: Y. Hey et al., IDENTIFICATION AND CLONING IN YEAST ARTIFICIAL CHROMOSOMES OF A REGION OF ELEVATED LOSS OF HETEROZYGOSITY ON CHROMOSOME 1P31.1, Cytogenetics and cell genetics, 72(2-3), 1996, pp. 148-148
STRONG LINKAGE DISEQUILIBRIUM AND HAPLOTYPE ANALYSIS IN JAPANESE PEDIGREES WITH MACHADO-JOSEPH DISEASE
Authors: ENDO K SASAKI H WAKISAKA A TANAKA H SAITO M IGARASHI S TAKIYAMA Y SANPEI K IWABUCHI K SUZUKI Y ONARI K SUZUKI T WEISSENBACH J WEBER JL NOMURA Y SEGAWA M NISHIZAWA M TSUJI S
Citation: K. Endo et al., STRONG LINKAGE DISEQUILIBRIUM AND HAPLOTYPE ANALYSIS IN JAPANESE PEDIGREES WITH MACHADO-JOSEPH DISEASE, American journal of medical genetics, 67(5), 1996, pp. 437-444
VARIABLE EXPRESSIVITY OF AUTOSOMAL-DOMINANT OPEN-ANGLE GLAUCOMA AT THE GLC1A LOCUS
Authors: RAYMOND V PLANTE M COTE G ANCTIL JL AMYOT M WEISSENBACH J MORISSETTE J
Citation: V. Raymond et al., VARIABLE EXPRESSIVITY OF AUTOSOMAL-DOMINANT OPEN-ANGLE GLAUCOMA AT THE GLC1A LOCUS, Investigative ophthalmology & visual science, 37(3), 1996, pp. 2079-2079
LANDING ON THE GENOME
Authors: WEISSENBACH J
Citation: J. Weissenbach, LANDING ON THE GENOME, Science, 274(5287), 1996, pp. 479-479
A GENE MAP OF THE HUMAN GENOME
Authors: SCHULER GD BOGUSKI MS STEWART EA STEIN LD GYAPAY G RICE K WHITE RE RODRIGUEZTOME P AGGARWAL A BAJOREK E BENTOLILA S BIRREN BB BUTLER A CASTLE AB CHIANNILKULCHAI N CHU A CLEE C COWLES S DAY PJR DIBLING T DROUOT N DUNHAM I DUPRAT S EAST C EDWARDS C FAN JB FANG N FIZAMES C GARRETT C GREEN L HADLEY D HARRIS M HARRISON P BRADY S HICKS A HOLLOWAY E HUI L HUSSAIN S LOUISDITSULLY C MA J MACGILVERY A MADER C MARATUKULAM A MATISE TC MCKUSICK KB MORISSETTE J MUNGALL A MUSELET D NUSBAUM HC PAGE DC PECK A PERKINS S PIERCY M QIN F QUACKENBUSH J RANBY S REIF T ROZEN S SANDERS C SHE X SILVA J SLONIM DK SODERLUND C SUN WL TABAR P THANGARAJAH T VEGACZAMY N VOLLRATH D VOYTICKY S WILMER T WU X ADAMS MD AUFFRAY C WALTER NAR BRANDON R DEHEJIA A GOODFELLOW PN HOULGATTE R HUDSON JR IDE SE IORIO KR LEE WY SEKI N NAGASE T ISHIKAWA K NOMURA N PHILLIPS C POLYMEROPOULOS MH SANDUSKY M SCHMITT K BERRY R SWANSON K TORRES R VENTER JC SIKELA JM BECKMANN JS WEISSENBACH J MYERS RM COX DR JAMES MR BENTLEY D DELOUKAS P LANDER ES HUDSON TJ
Citation: Gd. Schuler et al., A GENE MAP OF THE HUMAN GENOME, Science, 274(5287), 1996, pp. 540-546
GENOME MAPS .7. THE HUMAN TRANSCRIPT MAP
Authors: SCHULER GD BOGUSKI MS HUDSON TJ HUI L MA J CASTLE AB WU X SILVA J NUSBAUM HC BIRREN BB SLONIM DK ROZEN S STEIN LD PAGE D LANDER ES STEWART EA AGGARWAL A BAJOREK E BRADY S CHU A FANG N HADLEY D HARRIS M HUSSAIN S MARATUKULAM A PERKINS S PIERCY M QIN F REIF T SANDERS C SHE X SUN WL TABAR P VOYTICKY S MADER C MCKUSICK KB FAN JB COWLES S QUACKENBUSH J VOLLRATH D MYERS RM COX DR BUTLER A CLEE C DIBLING T EAST C EDWARDS C GARRETT C GREEN L HARRISON P HICKS A HOLLOWAY E RANBY S MACGILVERY A MUNGALL A PECK A WILMER T SODERLUND C RICE K DUNHAM I BENTLEY D DELOUKAS P GYAPAY G CHIANNILKULCHAI N FIZAMES C BENTOLILA S DUPRAT S VEGACZARNY N MUSELET D DROUOT N MORISSETTE J WEISSENBACH J MORISSETTE J JAMES MR WHITE RE THANGARAJAH T LOUISDITSULLY C DAY PJR GOODFELLOW PN SCHMITT K WALTER NAR BERRY R IORIO KR SIKELA JM POLYMEROPOULOS MH TORRES R IDE SE DEHEJIA A HOULGATTE R AUFFRAY C ADAMS MD PHILLIPS C BRANDON R SANDUSKY M VENTER JC SEKI N NAGASE T ISHIKAWA K NOMURA N RODRIGUEZTOME P MATISE TC LEE WY SWANSON KA HUDSON JR
Citation: Gd. Schuler et al., GENOME MAPS .7. THE HUMAN TRANSCRIPT MAP, Science, 274(5287), 1996, pp. 547-558
THE GENE RESPONSIBLE FOR ANDERMANN SYNDROME MAPS TO CHROMOSOME 15Q
Authors: MELANSON M CASAUBON L LOPESCENDES I MARINEAU C ANDERMANN E ANDERMANN F WEISSENBACH J MATHIEU J BOUCHARD JP PREVOST C ROULEAU GA
Citation: M. Melanson et al., THE GENE RESPONSIBLE FOR ANDERMANN SYNDROME MAPS TO CHROMOSOME 15Q, Neurology, 46(2), 1996, pp. 21005-21005
GENETIC SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS - THE ROLE OF MAG, MBP, MOG, OMGP, AND PLP
Authors: SEBOUN E CARSIQUE R PAHMDINH D BOESPFLUGTANGUY O GOODKIN DE LATHROP M RIMMLER J HAINES JL OKSENBERG J FIZAMES C LINCOLN R PERICAKVANCE MA GUSELLA JF ROSES AD WEISSENBACH J DAUTIGNY A HAUSER SL
Citation: E. Seboun et al., GENETIC SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS - THE ROLE OF MAG, MBP, MOG, OMGP, AND PLP, Neurology, 46(2), 1996, pp. 34004-34004
NOTCH3 MUTATIONS IN CADASIL, A HEREDITARY ADULT-ONSET CONDITION CAUSING STROKE AND DEMENTIA
Authors: JOUTEL A CORPECHOT C DUCROS A VAHEDI K CHABRIAT H MOUTON P ALAMOWITCH S DOMENGA V CECILLION M MARECHAL E MACIAZEK J VAYSSIERE C CRUAUD C CABANIS EA RUCHOUX MM WEISSENBACH J BACH JF BOUSSER MG TOURNIERLASSERVE E
Citation: A. Joutel et al., NOTCH3 MUTATIONS IN CADASIL, A HEREDITARY ADULT-ONSET CONDITION CAUSING STROKE AND DEMENTIA, Nature, 383(6602), 1996, pp. 707-710
A COMPREHENSIVE GENETIC-MAP OF THE HUMAN GENOME BASED ON 5,264 MICROSATELLITES
Authors: DIB C FAURE S FIZAMES C SAMSON D DROUOT N VIGNAL A MILLASSEAU P MARC S HAZAN J SEBOUN E LATHROP M GYAPAY G MORISSETTE J WEISSENBACH J
Citation: C. Dib et al., A COMPREHENSIVE GENETIC-MAP OF THE HUMAN GENOME BASED ON 5,264 MICROSATELLITES, Nature, 380(6570), 1996, pp. 152-154
MAPPING OF A SUSCEPTIBILITY LOCUS FOR CROHNS-DISEASE ON CHROMOSOME-16
Authors: HUGOT JP LAURENTPUIG P GOWERROUSSEAU C OLSON JM LEE JC BEAUGERIE L NAOM I DUPAS JL VANGOSSUM A ORHOLM M BONAITIPELLIE C WEISSENBACH J MATHEW CG LENNARDJONES JE CORTOT A COLOMBEL JF THOMAS G
Citation: Jp. Hugot et al., MAPPING OF A SUSCEPTIBILITY LOCUS FOR CROHNS-DISEASE ON CHROMOSOME-16, Nature, 379(6568), 1996, pp. 821-823
CLINICAL AND GENETIC-HETEROGENEITY OF HYPOCHONDROPLASIA
Authors: ROUSSEAU F BONAVENTURE J LEGEAIMALLET L SCHMIDT H WEISSENBACH J MAROTEAUX P MUNNICH A LEMERRER M
Citation: F. Rousseau et al., CLINICAL AND GENETIC-HETEROGENEITY OF HYPOCHONDROPLASIA, Journal of Medical Genetics, 33(9), 1996, pp. 749-752
APOLIPOPROTEIN-E GENOTYPE DOES NOT AFFECT AGE AT ONSET IN PATIENTS WITH CHROMOSOME-14 ENCODED ALZHEIMERS-DISEASE
Authors: BRICE A TARDIEU S DIDIERJEAN O LEGUERN E MICHON A PILLON B HAHN V DUBOIS B PENET C AGID Y CAMPION D MARTINEZ M BABRON MC CLERGETDARPOUX F BELLIS M CALANDA A HEILIG R WEISSENBACH J MALLET J FREBOURG T HANNEQUIN D PUEL M LEDOZE F PASQUIER F ZIMMERMANN MA THOMASANTERION C MOREAU O
Citation: A. Brice et al., APOLIPOPROTEIN-E GENOTYPE DOES NOT AFFECT AGE AT ONSET IN PATIENTS WITH CHROMOSOME-14 ENCODED ALZHEIMERS-DISEASE, Journal of Medical Genetics, 33(2), 1996, pp. 174-175
REFINED LOCALIZATION OF THE DARIERS-DISEASE AND SPINOCEREBELLAR ATAXIA TYPE-2 GENES AT CHROMOSOME 12Q24.1 - CONSTRUCTION OF A YAC CONTIG ENCOMPASSING THESE GENES
Authors: BRYCE SD CARTER SA PANG JT TWELLS R RENAULT B SCHLEICHNORTE B ALLOTEY R ROSS CJD KATSANTONIA E WEISSENBACH J KUCHERLAPATI RS REES JL MUNRO CS CHAMBERLAIN S STRACHAN T
Citation: Sd. Bryce et al., REFINED LOCALIZATION OF THE DARIERS-DISEASE AND SPINOCEREBELLAR ATAXIA TYPE-2 GENES AT CHROMOSOME 12Q24.1 - CONSTRUCTION OF A YAC CONTIG ENCOMPASSING THESE GENES, Journal of investigative dermatology, 107(3), 1996, pp. 210-210
PHENOTYPE OF AUTOSOMAL-DOMINANT SPASTIC PARAPLEGIA LINKED TO CHROMOSOME-2
Authors: DURR A DAVOINE CS PATERNOTTE C VONFELLENBERG J COGILNICEAN S COUTINHO P LAMY C BOURGEOIS S PRUDHOMME JF PENET C MAS JL BURGUNDER JM HAZAN J WEISSENBACH J BRICE A FONTAINE B
Citation: A. Durr et al., PHENOTYPE OF AUTOSOMAL-DOMINANT SPASTIC PARAPLEGIA LINKED TO CHROMOSOME-2, Brain, 119, 1996, pp. 1487-1496
PROGRESS IN THE SEARCH FOR SCHIZOPHRENIA SUSCEPTIBILITY GENES
Authors: MOISES HW YANG L KRISTBJARNARSON H BYERLEY W MACCIARDI F AROLT V BLACKWOOD D ASCHAUER HN HWU HG WEISSENBACH J SCHWINGER E GOTTESMAN II WETTERBERG L HELGASON T
Citation: Hw. Moises et al., PROGRESS IN THE SEARCH FOR SCHIZOPHRENIA SUSCEPTIBILITY GENES, Biological psychiatry, 39(7), 1996, pp. 394-394
SYSTEMATIC SCREENING OF THE ENTIRE GENOME IN RHEUMATOID-ARTHRITIS FAMILIES REVEALS 3 MAJOR SUSCEPTIBILITY LOCI
Authors: CORNELIS F FAURE S MARTINEZ M FRITZ P DIB C PRUDHOMME JF TRAN TH DELAYE A PRINCE N LEFEVRE C THOMAS G POIRIER M SOUBIGOU S ALIBERT O LASBLEIZ S FOUIX S LIOTE F LOSTE MN LEPAGE V CHARRON D GYAPAY G KUNTZ D BARDIN T WEISSENBACH J
Citation: F. Cornelis et al., SYSTEMATIC SCREENING OF THE ENTIRE GENOME IN RHEUMATOID-ARTHRITIS FAMILIES REVEALS 3 MAJOR SUSCEPTIBILITY LOCI, Arthritis and rheumatism, 39(9), 1996, pp. 280-280
RHEUMATOID-ARTHRITIS ASSOCIATION WITH A T-CELL RECEPTOR GENOTYPE
Authors: CORNELIS F HARDWICK L FLIPO RM MARTINEZ M LASBLEIZ S PRUDHOMME JF TRAN TH WALSH S DELAYE A NICOD A LOSTE MN LEPAGE V GIBSON K PILE K DJOULAH S DANZE PM LLOTE F CHARRON D WEISSENBACH J KUNTZ D BARDIN T WORDSWORTH BP
Citation: F. Cornelis et al., RHEUMATOID-ARTHRITIS ASSOCIATION WITH A T-CELL RECEPTOR GENOTYPE, Arthritis and rheumatism, 39(9), 1996, pp. 1428-1428
LINKAGE OF AN AMERICAN PEDIGREE WITH PALMOPLANTAR KERATODERMA AND MALIGNANCY (PALMOPLANTAR ECTODERMAL DYSPLASIA TYPE-III) TO 17Q24 - LITERATURE SURVEY AND PROPOSED UPDATED CLASSIFICATION OF THE KERATODERMAS
Authors: STEVENS HP KELSELL DP BRYANT SP BISHOP T SPURR NK WEISSENBACH J MARGER D MARGER RS LEIGH IM
Citation: Hp. Stevens et al., LINKAGE OF AN AMERICAN PEDIGREE WITH PALMOPLANTAR KERATODERMA AND MALIGNANCY (PALMOPLANTAR ECTODERMAL DYSPLASIA TYPE-III) TO 17Q24 - LITERATURE SURVEY AND PROPOSED UPDATED CLASSIFICATION OF THE KERATODERMAS, Archives of dermatology, 132(6), 1996, pp. 640-651
EUROPEAN GENE-MAPPING PROJECT (EUROGEM) - BREAKPOINT PANELS FOR HUMAN-CHROMOSOMES BASED ON THE CEPH REFERENCE FAMILIES
Authors: COX SA ATTWOOD J BRYANT SP BAINS R POVEY R POVEY S REBELLO M KAPSETAKI M MOSCHONAS NK GRZESCHIK KH OTTO M DIXON M SUDWORTH HE KOOY RF WRIGHT A TEAGUE P TERRENATO L VERGNAUD G MONFOUILLOUX S WEISSENBACH J ALIBERT O DIB C FAURE S BAKKER E PEARSON NM VOSSEN RHAM GAL A MUELLERMYHSOK B CANN HM SPURR NK
Citation: Sa. Cox et al., EUROPEAN GENE-MAPPING PROJECT (EUROGEM) - BREAKPOINT PANELS FOR HUMAN-CHROMOSOMES BASED ON THE CEPH REFERENCE FAMILIES, Annals of Human Genetics, 60, 1996, pp. 447-486
AGE AND ORIGIN OF 2 COMMON MLH1 MUTATIONS PREDISPOSING TO HEREDITARY COLON-CANCER
Authors: MOISIO AL SISTONEN P WEISSENBACH J DELACHAPELLE A PELTOMAKI P
Citation: Al. Moisio et al., AGE AND ORIGIN OF 2 COMMON MLH1 MUTATIONS PREDISPOSING TO HEREDITARY COLON-CANCER, American journal of human genetics, 59(6), 1996, pp. 1243-1251
THE GENE FOR AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-II IS LOCATED IN A 5-CM REGION IN 3P12-P13 - GENETIC AND PHYSICAL MAPPING OF THE SCA7 LOCUS
Authors: DAVID G ABBAS N COULLIN P STEVANIN G HORTA W GEMMILL R WEISSENBACH J WOOD N CUNHA S DRABKIN H HARDING AE AGID Y BRICE A
Citation: G. David et al., THE GENE FOR AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-II IS LOCATED IN A 5-CM REGION IN 3P12-P13 - GENETIC AND PHYSICAL MAPPING OF THE SCA7 LOCUS, American journal of human genetics, 59(6), 1996, pp. 1328-1336
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