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Results: 1-17 |
Results: 17
OVARIAN-CANCER RISK IN BRCA1 CARRIERS IS MODIFIED BY THE HRAS1 VARIABLE NUMBER OF TANDEM REPEAT (VNTR) LOCUS
Authors: PHELAN CM REBBECK TR WEBER BL DEVILEE P RUTTLEDGE MH LYNCH HT LENOIR GM STRATTON MR EASTON DF PONDER BAJ CANNONALBRIGHT L LARSSON C GOLDGAR DE NAROD SA
Citation: Cm. Phelan et al., OVARIAN-CANCER RISK IN BRCA1 CARRIERS IS MODIFIED BY THE HRAS1 VARIABLE NUMBER OF TANDEM REPEAT (VNTR) LOCUS, Nature genetics, 12(3), 1996, pp. 309-311
THE HUMAN MAMMARY-DERIVED GROWTH INHIBITOR (MDGI) GENE - GENOMIC STRUCTURE AND MUTATION ANALYSIS IN HUMAN BREAST-TUMORS (VOL 34, PG 63, 1996)
Authors: PHELAN CM LARSSON C BAIRD S FUTREAL PA RUTTLEDGE MH MORGAN K TONIN P HUNG H KORNELUK RG POLLAK MN NAROD SA
Citation: Cm. Phelan et al., THE HUMAN MAMMARY-DERIVED GROWTH INHIBITOR (MDGI) GENE - GENOMIC STRUCTURE AND MUTATION ANALYSIS IN HUMAN BREAST-TUMORS (VOL 34, PG 63, 1996), Genomics, 36(2), 1996, pp. 377-377
THE HUMAN MAMMARY-DERIVED GROWTH INHIBITOR (MDGI) GENE - GENOMIC STRUCTURE AND MUTATION ANALYSIS IN HUMAN BREAST-TUMORS
Authors: PHELAN CM LARSSON C BAIRD S FUTREAL PA RUTTLEDGE MH MORGAN K TONIN P HUNG H KORNELUK RG POLLAK MN NAROD SA
Citation: Cm. Phelan et al., THE HUMAN MAMMARY-DERIVED GROWTH INHIBITOR (MDGI) GENE - GENOMIC STRUCTURE AND MUTATION ANALYSIS IN HUMAN BREAST-TUMORS, Genomics, 34(1), 1996, pp. 63-68
LOSS OF HETEROZYGOSITY ON CHROMOSOME-22 IN HUMAN GLIOMAS DOES NOT INACTIVATE THE NEUROFIBROMATOSIS TYPE-2 GENE
Authors: WATKINS D RUTTLEDGE MH SARRAZIN J RANGARATNAM S POISSON M DELATTRE JY ROULEAU GA
Citation: D. Watkins et al., LOSS OF HETEROZYGOSITY ON CHROMOSOME-22 IN HUMAN GLIOMAS DOES NOT INACTIVATE THE NEUROFIBROMATOSIS TYPE-2 GENE, Cancer genetics and cytogenetics, 92(1), 1996, pp. 73-78
TYPE OF MUTATION IN THE NEUROFIBROMATOSIS TYPE-2 GENE (NF2) FREQUENTLY DETERMINES SEVERITY OF DISEASE
Authors: RUTTLEDGE MH ANDERMANN AA PHELAN CM CLAUDIO JO HAN FY CHRETIEN N RANGARATNAM S MACCOLLIN M SHORT P PARRY D MICHELS V RICCARDI VM WEKSBERG R KITAMURA K BRADBURN JM HALL BD PROPPING P ROULEAU GA
Citation: Mh. Ruttledge et al., TYPE OF MUTATION IN THE NEUROFIBROMATOSIS TYPE-2 GENE (NF2) FREQUENTLY DETERMINES SEVERITY OF DISEASE, American journal of human genetics, 59(2), 1996, pp. 331-342
GENOTYPE-PHENOTYPE CORRELATION IN NEUROFIBROMATOSIS TYPE-2 PATIENTS
Authors: ANDERMANN AA RUTTLEDGE MH RANGARATNAM S ROULEAU GA
Citation: Aa. Andermann et al., GENOTYPE-PHENOTYPE CORRELATION IN NEUROFIBROMATOSIS TYPE-2 PATIENTS, Annals of neurology, 38(3), 1995, pp. 537-537
CHROMOSOME-17 ABNORMALITIES AND LACK OF TP53 MUTATIONS IN PEDIATRIC CENTRAL-NERVOUS-SYSTEM TUMORS
Authors: PHELAN CM LIU L RUTTLEDGE MH MUNTZNING K RIDDERHEIM PA COLLINS VP
Citation: Cm. Phelan et al., CHROMOSOME-17 ABNORMALITIES AND LACK OF TP53 MUTATIONS IN PEDIATRIC CENTRAL-NERVOUS-SYSTEM TUMORS, Human genetics, 96(6), 1995, pp. 684-690
MACHADO-JOSEPH-DISEASE MAPS TO THE SAME REGION OF CHROMOSOME-14 AS THE SPINOCEREBELLAR ATAXIA TYPE-3 LOCUS
Authors: TWIST EC CASAUBON LK RUTTLEDGE MH RAO VS MACLEOD PM RADVANY J ZHAO ZY ROSENBERG RN FARRER LA ROULEAU GA
Citation: Ec. Twist et al., MACHADO-JOSEPH-DISEASE MAPS TO THE SAME REGION OF CHROMOSOME-14 AS THE SPINOCEREBELLAR ATAXIA TYPE-3 LOCUS, Journal of Medical Genetics, 32(1), 1995, pp. 25-31
EVIDENCE FOR THE COMPLETE INACTIVATION OF THE NF2 GENE IN THE MAJORITY OF SPORADIC MENINGIOMAS
Authors: RUTTLEDGE MH SARRAZIN J RANGARATNAM S PHELAN CM TWIST E MEREL P DELATTRE O THOMAS G NORDENSKJOLD M COLLINS VP DUMANSKI JP ROULEAU GA
Citation: Mh. Ruttledge et al., EVIDENCE FOR THE COMPLETE INACTIVATION OF THE NF2 GENE IN THE MAJORITY OF SPORADIC MENINGIOMAS, Nature genetics, 6(2), 1994, pp. 180-184
DELETIONS ON CHROMOSOME-22 IN SPORADIC MENINGIOMA
Authors: RUTTLEDGE MH XIE YG HAN FY PEYRARD M COLLINS VP NORDENSKJOLD M DUMANSKI JP
Citation: Mh. Ruttledge et al., DELETIONS ON CHROMOSOME-22 IN SPORADIC MENINGIOMA, Genes, chromosomes & cancer, 10(2), 1994, pp. 122-130
CHARACTERIZATION OF A NEW MEMBER OF THE HUMAN BETA-ADAPTIN GENE FAMILY FROM CHROMOSOME 22Q12, A CANDIDATE MENINGIOMA GENE
Authors: PEYRARD M FRANSSON I XIE YG HAN FY RUTTLEDGE MH SWAHN S COLLINS JE DUNHAM I COLLINS VP DUMANSKI JP
Citation: M. Peyrard et al., CHARACTERIZATION OF A NEW MEMBER OF THE HUMAN BETA-ADAPTIN GENE FAMILY FROM CHROMOSOME 22Q12, A CANDIDATE MENINGIOMA GENE, Human molecular genetics, 3(8), 1994, pp. 1393-1399
THE NEUROFIBROMATOSIS TYPE-2 GENE IS INACTIVATED IN SCHWANNOMAS
Authors: TWIST EC RUTTLEDGE MH ROUSSEAU M SANSON M PAPI L MEREL P DELATTRE O THOMAS G ROULEAU GA
Citation: Ec. Twist et al., THE NEUROFIBROMATOSIS TYPE-2 GENE IS INACTIVATED IN SCHWANNOMAS, Human molecular genetics, 3(1), 1994, pp. 147-151
PHYSICAL MAPPING OF THE NF2 MENINGIOMA REGION ON HUMAN-CHROMOSOME 22Q12/
Authors: RUTTLEDGE MH XIE YG HAN FY GIOVANNINI M JANSON M FRANSSON I WERELIUS B DELATTRE O THOMAS G EVANS G DUMANSKI JP
Citation: Mh. Ruttledge et al., PHYSICAL MAPPING OF THE NF2 MENINGIOMA REGION ON HUMAN-CHROMOSOME 22Q12/, Genomics, 19(1), 1994, pp. 52-59
CLONING OF A NOVEL, ANONYMOUS GENE FROM A MEGABASE-RANGE YAC AND COSMID CONTIG IN THE NEUROFIBROMATOSIS TYPE-2 MENINGIOMA REGION ON HUMAN CHROMOSOME-22Q12
Authors: XIE YG HAN FY PEYRARD M RUTTLEDGE MH FRANSSON I DEJONG P COLLINS J DUNHAM I NORDENSKJOLD M DUMANSKI JP
Citation: Yg. Xie et al., CLONING OF A NOVEL, ANONYMOUS GENE FROM A MEGABASE-RANGE YAC AND COSMID CONTIG IN THE NEUROFIBROMATOSIS TYPE-2 MENINGIOMA REGION ON HUMAN CHROMOSOME-22Q12, Human molecular genetics, 2(9), 1993, pp. 1361-1368
PRESYMPTOMATIC DIAGNOSIS FOR NEUROFIBROMATOSIS-2 WITH CHROMOSOME-22 MARKERS
Authors: RUTTLEDGE MH NAROD SA DUMANSKI JP PARRY DM ELDRIDGE R WERTELECKI W PARBOOSINGH J FAUCHER MC LENOIR GM COLLINS VP NORDENSKJOLD M ROULEAU GA
Citation: Mh. Ruttledge et al., PRESYMPTOMATIC DIAGNOSIS FOR NEUROFIBROMATOSIS-2 WITH CHROMOSOME-22 MARKERS, Neurology, 43(9), 1993, pp. 1753-1760
ANALYSIS OF THE NF2-GENE IN TUMORS SHOWING LOSS OF HETEROZYGOSITY ON CHROMOSOME-22
Authors: ROULEAU GA TWIST EC RUTTLEDGE MH ROUSSEAU M SARAZIN J MARINEAU C DELLATRE O THOMAS G
Citation: Ga. Rouleau et al., ANALYSIS OF THE NF2-GENE IN TUMORS SHOWING LOSS OF HETEROZYGOSITY ON CHROMOSOME-22, American journal of human genetics, 53(3), 1993, pp. 351-351
CONSTRUCTION OF YAC AND COSMID CONTIG IN THE NEUROFIBROMATOSIS TYPE-2(NF2) AND MENINGIOMA REGION ON CHROMOSOME-22Q12
Authors: XIE YG HAN FY RUTTLEDGE MH FRANSSON I PEYRARD M DUNHAM I COLLINS J DEJONG P NORDENSKJOLD M DUMANSKI JP
Citation: Yg. Xie et al., CONSTRUCTION OF YAC AND COSMID CONTIG IN THE NEUROFIBROMATOSIS TYPE-2(NF2) AND MENINGIOMA REGION ON CHROMOSOME-22Q12, American journal of human genetics, 53(3), 1993, pp. 1375-1375
Risultati: 1-17 |