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Results: 1-25 | 26-50 | 51-54
Results: 1-25/54
ALLELIC IMBALANCE, INCLUDING DELETION OF PTEN MMACI, AT THE COWDEN DISEASE LOCUS ON 10Q22-23, IN HAMARTOMAS FROM PATIENTS WITH COWDEN SYNDROME AND GERMLINE PTEN MUTATION/
Authors: MARSH DJ DAHIA PLM COULON V ZHENG ZM DORIONBONNET F CALL KM LITTLE R LIN AY EELES RA GOLDSTEIN AM HODGSON SV RICHARDSON AL ROBINSON BG WEBER HC LONGY M ENG C
Citation: Dj. Marsh et al., ALLELIC IMBALANCE, INCLUDING DELETION OF PTEN MMACI, AT THE COWDEN DISEASE LOCUS ON 10Q22-23, IN HAMARTOMAS FROM PATIENTS WITH COWDEN SYNDROME AND GERMLINE PTEN MUTATION/, Genes, chromosomes & cancer, 21(1), 1998, pp. 61-69
A STUDY OF THE FREQUENCY OF GERMLINE ATAXIA-TELANGIECTASIA MUTATED MUTATIONS IN YOUNG BREAST-CANCER PATIENTS
Authors: IZATT L HODGSON SV SOLOMON E
Citation: L. Izatt et al., A STUDY OF THE FREQUENCY OF GERMLINE ATAXIA-TELANGIECTASIA MUTATED MUTATIONS IN YOUNG BREAST-CANCER PATIENTS, European journal of human genetics, 6, 1998, pp. 604-604
MUTATION SPECTRUM AND GENOTYPE-PHENOTYPE ANALYSES IN COWDEN-DISEASE AND BANNAYAN-ZONANA-SYNDROME, 2 HAMARTOMA SYNDROMES WITH GERMLINE PTEN MUTATION
Authors: MARSH DJ COULON V LUNETTA KL ROCCASERRA P DAHIA PLM ZHENG ZM LIAW D CARON S DUBOUE B LIN AY RICHARDSON AL BONNETBLANC JM BRESSIEUX JM CABARROTMOREAU A CHOMPRET A DEMANGE L EELES RA YAHANDA AM FEARON ER FRICKER JP GORLIN RJ HODGSON SV HUSON S LACOMBE D LEPRAT F ODENT S TOULOUSE C OLOPADE OI SOBOL H TISHLER S WOODS CG ROBINSON BG WEBER HC PARSONS R PEACOCKE M LONGY M ENG C
Citation: Dj. Marsh et al., MUTATION SPECTRUM AND GENOTYPE-PHENOTYPE ANALYSES IN COWDEN-DISEASE AND BANNAYAN-ZONANA-SYNDROME, 2 HAMARTOMA SYNDROMES WITH GERMLINE PTEN MUTATION, Human molecular genetics, 7(3), 1998, pp. 507-515
THE APC VARIANTS I1307K AND E1317Q ARE ASSOCIATED WITH COLORECTAL TUMORS, BUT NOT ALWAYS WITH A FAMILY HISTORY
Authors: FRAYLING IM BECK NE ILYAS M DOVEEDWIN I GOODMAN P PACK K BELL JA WILLIAMS CB HODGSON SV THOMAS HJW TALBOT IC BODMER WF TOMLINSON IPM
Citation: Im. Frayling et al., THE APC VARIANTS I1307K AND E1317Q ARE ASSOCIATED WITH COLORECTAL TUMORS, BUT NOT ALWAYS WITH A FAMILY HISTORY, Proceedings of the National Academy of Sciences of the United Statesof America, 95(18), 1998, pp. 10722-10727
A SURVEY OF PHENOTYPIC FEATURES IN JUVENILE POLYPOSIS
Authors: DESAI DC MURDAY V PHILLIPS RKS NEALE KF MILLA P HODGSON SV
Citation: Dc. Desai et al., A SURVEY OF PHENOTYPIC FEATURES IN JUVENILE POLYPOSIS, Journal of Medical Genetics, 35(6), 1998, pp. 476-481
EVIDENCE OF LINKAGE OF THE INFLAMMATORY BOWEL-DISEASE SUSCEPTIBILITY LOCUS ON CHROMOSOME-16 (IBD1) TO ULCERATIVE-COLITIS
Authors: MIRZA MM LEE J TEARE D HUGOT JP LAURENTPUIG P COLOMBEL JF HODGSON SV THOMAS G EASTON DF LENNARDJONES JE MATHEW CG
Citation: Mm. Mirza et al., EVIDENCE OF LINKAGE OF THE INFLAMMATORY BOWEL-DISEASE SUSCEPTIBILITY LOCUS ON CHROMOSOME-16 (IBD1) TO ULCERATIVE-COLITIS, Journal of Medical Genetics, 35(3), 1998, pp. 218-221
GERMLINE PTEN MUTATIONS IN COWDEN-SYNDROME-LIKE FAMILIES
Authors: MARSH DJ DAHIA PLM CARON S KUM JB FRAYLING IM TOMLINSON IPM HUGHES KS EELES RA HODGSON SV MURDAY VA HOULSTON R ENG C
Citation: Dj. Marsh et al., GERMLINE PTEN MUTATIONS IN COWDEN-SYNDROME-LIKE FAMILIES, Journal of Medical Genetics, 35(11), 1998, pp. 881-885
THE GENETICS OF LEARNING-DISABILITIES
Authors: HODGSON SV
Citation: Sv. Hodgson, THE GENETICS OF LEARNING-DISABILITIES, Developmental Medicine and Child Neurology, 40(2), 1998, pp. 137-140
DELETION OF CHROMOSOME 3Q PROXIMAL REGION GIVES RISE TO A VARIABLE PHENOTYPE
Authors: OGILVIE CM ROONEY SC HODGSON SV BERRY AC
Citation: Cm. Ogilvie et al., DELETION OF CHROMOSOME 3Q PROXIMAL REGION GIVES RISE TO A VARIABLE PHENOTYPE, Clinical genetics, 53(3), 1998, pp. 220-222
FAMILY HISTORY AND SURVIVAL IN PREMENOPAUSAL BREAST-CANCER
Authors: MOHAMMED SN SMITH P HODGSON SV FENTIMAN IS MILES DW BARNES DM MILLIS RR RUBENS RD
Citation: Sn. Mohammed et al., FAMILY HISTORY AND SURVIVAL IN PREMENOPAUSAL BREAST-CANCER, British Journal of Cancer, 77(12), 1998, pp. 2252-2256
MOLECULAR AND CLINICOPATHOLOGICAL FEATURES OF 2 FAMILIES WITH THE HNPCC SYNDROME AND UNUSUAL PHENOTYPES
Authors: TOMLINSON IPM BECK NE HOMFRAY T HAROCOPOS CJ ADAMS M HODGSON SV MARKIE D BODMER WF
Citation: Ipm. Tomlinson et al., MOLECULAR AND CLINICOPATHOLOGICAL FEATURES OF 2 FAMILIES WITH THE HNPCC SYNDROME AND UNUSUAL PHENOTYPES, GI cancer, 2(2), 1997, pp. 89-98
GENETIC SUSCEPTIBILITY TO BREAST AND OVARIAN-CANCER
Authors: HODGSON SV
Citation: Sv. Hodgson, GENETIC SUSCEPTIBILITY TO BREAST AND OVARIAN-CANCER, Cancer gene therapy, 4(1), 1997, pp. 67-68
USE OF SSCP ANALYSIS TO IDENTIFY GERMLINE MUTATIONS IN HNPCC FAMILIESFULFILLING THE AMSTERDAM CRITERIA
Authors: BECK NE TOMLINSON IPM HOMFRAY T FRAYLING I HODGSON SV HAROCOPOS C BODMER WF
Citation: Ne. Beck et al., USE OF SSCP ANALYSIS TO IDENTIFY GERMLINE MUTATIONS IN HNPCC FAMILIESFULFILLING THE AMSTERDAM CRITERIA, Human genetics, 99(2), 1997, pp. 219-224
CLINICAL-FEATURES AND MOLECULAR ANALYSIS OF A FAMILY WITH MULTIPLE COLON TUMORS AND REDUCED PLASMINOGEN-ACTIVATOR ACTIVITY
Authors: TOMLINSON IPM BECK NE WILLIAMSON J HAROCOPOS CJ MITCHELL VE HODGSON SV BODMER WF
Citation: Ipm. Tomlinson et al., CLINICAL-FEATURES AND MOLECULAR ANALYSIS OF A FAMILY WITH MULTIPLE COLON TUMORS AND REDUCED PLASMINOGEN-ACTIVATOR ACTIVITY, International journal of colorectal disease, 12(1), 1997, pp. 1-3
FAMILIAL ADENOMATOUS POLYPOSIS PRESENTING WITH CHILDHOOD DESMOIDS
Authors: CLARK SK PACK K PRITCHARD J HODGSON SV
Citation: Sk. Clark et al., FAMILIAL ADENOMATOUS POLYPOSIS PRESENTING WITH CHILDHOOD DESMOIDS, Lancet, 349(9050), 1997, pp. 471-472
FREQUENCY OF GERMLINE HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER GENE-MUTATIONS IN PATIENTS WITH MULTIPLE OR EARLY-ONSET COLORECTAL ADENOMAS
Authors: BECK NE TOMLINSON IPM HOMFRAY TFR FRAYLING IM HODGSON SV BODMER WF
Citation: Ne. Beck et al., FREQUENCY OF GERMLINE HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER GENE-MUTATIONS IN PATIENTS WITH MULTIPLE OR EARLY-ONSET COLORECTAL ADENOMAS, Gut, 41(2), 1997, pp. 235-238
DETERMINATION OF THE CLONALITY OF COLORECTAL TUMORS - CLUES TO THE ORIGIN OF HUMAN CANCER
Authors: NOVELLI MR WILLIAMSON JA TOMLINSON IPM ELIA G HODGSON SV TALBOT IC BODMER WF WRIGHT NA
Citation: Mr. Novelli et al., DETERMINATION OF THE CLONALITY OF COLORECTAL TUMORS - CLUES TO THE ORIGIN OF HUMAN CANCER, Gut, 40, 1997, pp. 177-177
CLINICAL AND MOLECULAR-FEATURES OF THE HEREDITARY MIXED POLYPOSIS SYNDROME
Authors: WHITELAW SC MURDAY VA TOMLINSON IPM THOMAS HJW COTTRELL S GINSBERG A BUKOFZER S HODGSON SV SKUDOWITZ RB JASS JR TALBOT IC NORTHOVER JMA BODMER WF SOLOMON E
Citation: Sc. Whitelaw et al., CLINICAL AND MOLECULAR-FEATURES OF THE HEREDITARY MIXED POLYPOSIS SYNDROME, Gastroenterology, 112(2), 1997, pp. 327-334
REGIONAL PROLIFERATIVE PATTERNS IN THE COLON OF PATIENTS AT RISK FOR HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER
Authors: PATCHETT SE ALSTEAD EM SAUNDERS BP HODGSON SV FARTHING MJG
Citation: Se. Patchett et al., REGIONAL PROLIFERATIVE PATTERNS IN THE COLON OF PATIENTS AT RISK FOR HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER, Diseases of the colon & rectum, 40(2), 1997, pp. 168-171
EXCLUSION OF PTEN AND 10Q22-24 AS THE SUSCEPTIBILITY LOCUS FOR JUVENILE POLYPOSIS SYNDROME
Authors: MARSH DJ ROTH S LUNETTA KL HEMMINKI A DAHIA PLM SISTONEN P ZHENG ZM CARON S VANORSOUW NJ BODMER WF COTTRELL SE DUNLOP MG ECCLES D HODGSON SV JARVINEN H KELLOKUMPU I MARKIE D NEALE K PHILLIPS R ROZEN P SYNGAL S VIJG J TOMLINSON IPM AALTONEN LA ENG C
Citation: Dj. Marsh et al., EXCLUSION OF PTEN AND 10Q22-24 AS THE SUSCEPTIBILITY LOCUS FOR JUVENILE POLYPOSIS SYNDROME, Cancer research, 57(22), 1997, pp. 5017-5021
GENETIC TESTING IS IMPORTANT IN FAMILIES WITH A HISTORY SUGGESTIVE OFHEREDITARY NONPOLYPOSIS COLORECTAL-CANCER EVEN IF THE AMSTERDAM CRITERIA ARE NOT FULFILLED
Authors: BECK NE TOMLINSON IPM HOMFRAY T HODGSON SV HAROCOPOS CJ BODMER WF
Citation: Ne. Beck et al., GENETIC TESTING IS IMPORTANT IN FAMILIES WITH A HISTORY SUGGESTIVE OFHEREDITARY NONPOLYPOSIS COLORECTAL-CANCER EVEN IF THE AMSTERDAM CRITERIA ARE NOT FULFILLED, British Journal of Surgery, 84(2), 1997, pp. 233-237
PAROXYSMAL DYSTONIC CHOREOATHETOSIS - GENETIC-LINKAGE STUDIES IN A BRITISH FAMILY
Authors: JARMAN PR DAVIS MB HODGSON SV MARSDEN CD WOOD NW
Citation: Pr. Jarman et al., PAROXYSMAL DYSTONIC CHOREOATHETOSIS - GENETIC-LINKAGE STUDIES IN A BRITISH FAMILY, Brain, 120, 1997, pp. 2125-2130
FAMILIAL INFILTRATIVE FIBROMATOSIS (DESMOID TUMORS) (MIM135290) CAUSED BY A RECURRENT 3'-APC GENE MUTATION
Authors: SCOTT RJ FROGGATT NJ TREMBATH RC EVANS DGR HODGSON SV MAHER ER
Citation: Rj. Scott et al., FAMILIAL INFILTRATIVE FIBROMATOSIS (DESMOID TUMORS) (MIM135290) CAUSED BY A RECURRENT 3'-APC GENE MUTATION, Human molecular genetics, 5(12), 1996, pp. 1921-1924
POLYCLONAL ORIGIN OF COLONIC ADENOMAS IN AN XO XY PATIENT WITH FAP/
Authors: NOVELLI MR WILLIAMSON JA TOMLINSON IPM ELIA G HODGSON SV TALBOT IC BODMER WF WRIGHT NA
Citation: Mr. Novelli et al., POLYCLONAL ORIGIN OF COLONIC ADENOMAS IN AN XO XY PATIENT WITH FAP/, Science, 272(5265), 1996, pp. 1187-1190
BREAST-CANCER AND BRCA1 MUTATIONS
Authors: MATHEW CG SOLOMON E HODGSON SV
Citation: Cg. Mathew et al., BREAST-CANCER AND BRCA1 MUTATIONS, The New England journal of medicine, 334(18), 1996, pp. 1198-1198
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