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Results: 1-25/40
Authors:
BAILEY DMD
BARRETT T
BUTLER A
HARRISON R
BARTON DE
Citation: Dmd. Bailey et al., ABSENCE OF DAZ (DELETED IN AZOOSPERMIA) GENE IN A FERTILE MAN AND HISINFERTILE SON, European journal of human genetics, 6, 1998, pp. 4226-4226
Authors:
RYAN F
DEVANEY D
JOYCE C
NESTOROWICZ A
PERMUTT MA
GLASER B
BARTON DE
THORNTON PS
Citation: F. Ryan et al., HYPERINSULINISM - MOLECULAR ETIOLOGY OF FOCAL DISEASE, Archives of Disease in Childhood, 79(5), 1998, pp. 445-447
Authors:
BARTON DE
Citation: De. Barton, GENETIC SERVICES IN IRELAND, European journal of human genetics, 5, 1997, pp. 100-104
Authors:
IRVING RM
MOFFAT DA
HARDY DG
BARTON DE
XUEREB JH
HOLLAND FJ
MAHER ER
Citation: Rm. Irving et al., A MOLECULAR, CLINICAL, AND IMMUNOHISTOCHEMICAL STUDY OF VESTIBULAR SCHWANNOMA, Otolaryngology and head and neck surgery, 116(4), 1997, pp. 426-430
Authors:
GREGORY GA
WOOLF DA
MCMAHON R
MAHER ER
BARTON DE
Citation: Ga. Gregory et al., CYSTIC-FIBROSIS DIAGNOSED BY MOLECULAR-GENETIC INVESTIGATION IN THE MOTHER OF A PATIENT WITH CYSTIC-FIBROSIS, Thorax, 52(1), 1997, pp. 96-97
Authors:
DOW DJ
RUBINSZTEIN DC
YATES JRW
BARTON DE
FERGUSONSMITH MA
Citation: Dj. Dow et al., INSTABILITY OF NORMAL (CTG)(N) ALLELES IN THE DM KINASE GENE, Journal of Medical Genetics, 34(10), 1997, pp. 871-873
Authors:
MCCABE D
RYAN F
MURPHY R
BARTON DE
Citation: D. Mccabe et al., FRIEDREICH-ATAXIA WITHOUT GAA EXPANSIONS EXPANSIONS WITHOUT FRIEDREICH-ATAXIA, Journal of Medical Genetics, 34, 1997, pp. 60-60
Authors:
JOYCE C
WOODHEAD H
COSTIGAN C
BARTON DE
Citation: C. Joyce et al., UNIPARENTAL DISOMY IN SILVER-RUSSELL-SYNDROME AND PRIMORDIAL GROWTH-RETARDATION - LESS COMMON THAN PREVIOUSLY REPORTED, Journal of Medical Genetics, 34, 1997, pp. 544-544
Authors:
BULL LN
VANEIJK MJT
LIAO M
PAWLIKOWSKA L
DEYOUNG J
STRICKER N
JUIJN JA
CARLTON V
TYGSTRUP N
WHITINGTON P
BARTON DE
BOURKE B
PAWLOWSKA J
JANKOWSKA I
LOMRI N
SCHARSCHMIDT B
BERGER R
KNISELY AS
HOUWEN RHJ
FREIMER NB
Citation: Ln. Bull et al., LOCALIZATION OF THE BRIC PFIC1 GENE TO A 250 KB INTERVAL THROUGH HAPLOTYPE ANALYSIS/, American journal of human genetics, 61(4), 1997, pp. 1569-1569
Authors:
HARADA T
IRVING RM
XUEREB JH
BARTON DE
HARDY DG
MOFFAT DA
MAHER ER
Citation: T. Harada et al., MOLECULAR-GENETIC INVESTIGATION OF THE NEUROFIBROMATOSIS TYPE-2 TUMOR-SUPPRESSOR GENE IN SPORADIC MENINGIOMA, Journal of neurosurgery, 84(5), 1996, pp. 847-851
Authors:
GEORGE NDL
PAYNE SJ
BILL RM
BARTON DE
MOORE AT
YATES JRW
Citation: Ndl. George et al., IMPROVED GENETIC-MAPPING OF X-LINKED RETINOSCHISIS, Journal of Medical Genetics, 33(11), 1996, pp. 919-922
Authors:
SCHWARZ MJ
MALONE GM
HAWORTH A
CHEADLE JP
MEREDITH AL
GARDNER A
SAWYER IH
CONNARTY M
DENNIS N
SELLER A
HARRIS A
TAYLOR R
DEAR S
MIDDLETONPRICE H
MCMAHON C
MAYALL E
MCMAHON R
BARTON DE
GILES M
LINDLEY V
PLAHA DS
PRICE S
SHARIF A
CROSS GS
DALTON A
TAYLOR G
WALLACE A
TASSABEHJI M
WHITTAKER JL
BUTLER R
CURTIS A
PINKETT R
GILFILLAN AJ
BROCK DJH
HIGGINS GS
LANYON G
MIEDZYBRODZKA Z
DAVIDSON M
GRAHAM CA
HILL AJM
Citation: Mj. Schwarz et al., CYSTIC-FIBROSIS MUTATION ANALYSIS - REPORT FROM 22 UK REGIONAL GENETICS LABORATORIES, Human mutation, 6(4), 1995, pp. 326-333
Authors:
RUBINSZTEIN DC
LEGGO J
GOODBURN S
BARTON DE
FERGUSONSMITH MA
Citation: Dc. Rubinsztein et al., HAPLOTYPE ANALYSIS OF THE DELTA-2642 AND (CAG)(N) POLYMORPHISMS IN THE HUNTINGTONS-DISEASE (HD) GENE PROVIDES AN EXPLANATION FOR AN APPARENT FOUNDER HD HAPLOTYPE, Human molecular genetics, 4(2), 1995, pp. 203-206
Authors:
RUBINSZTEIN DC
LEGGO J
GOODBURN S
BARTON DE
FERGUSONSMITH MA
Citation: Dc. Rubinsztein et al., NORMAL CAG AND CCG REPEATS IN THE HUNTINGTONS-DISEASE GENES OF PARKINSONS-DISEASE PATIENTS, American journal of medical genetics, 60(2), 1995, pp. 109-110
Authors:
FROGGATT NJ
JOYCE JA
DAVIES R
EVANS DGR
PONDER BAJ
BARTON DE
MAHER ER
Citation: Nj. Froggatt et al., A FREQUENT HMSH2 MUTATION IN HEREDITARY NONPOLYPOSIS COLON-CANCER SYNDROME, Lancet, 345(8951), 1995, pp. 727-727
Authors:
FROGGATT NJ
KOCH J
DAVIES R
EVANS DGR
CLAMP A
QUARRELL OWJ
WEISSENBACH J
HODGSON SV
PONDER BAJ
BARTON DE
MAHER ER
Citation: Nj. Froggatt et al., GENETIC-LINKAGE ANALYSIS IN HEREDITARY NONPOLYPOSIS COLON-CANCER SYNDROME, Journal of Medical Genetics, 32(5), 1995, pp. 352-357
Authors:
RUBINSZTEIN DC
AMOS W
LEGGO J
GOODBURN S
RAMESAR RS
OLD J
BONTROP R
MCMAHON R
BARTON DE
FERGUSONSMITH MA
Citation: Dc. Rubinsztein et al., MUTATIONAL BIAS PROVIDES A MODEL FOR THE EVOLUTION OF HUNTINGTONS-DISEASE AND PREDICTS A GENERAL INCREASE IN DISEASE PREVALENCE, Journal of Medical Genetics, 32(2), 1995, pp. 142-142
Authors:
FROGGATT NJ
KOCH DJ
DAVIES R
EVANS DGR
PARSONS R
VOGELSTEIN B
HODGSON SV
PONDER BAJ
BARTON DE
MAHER ER
Citation: Nj. Froggatt et al., MOLECULAR-GENETIC ANALYSIS OF HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER SYNDROME, Journal of Medical Genetics, 32(2), 1995, pp. 146-146
Authors:
DOW DJ
RUBINSZTEIN DC
FERGUSONSMITH MA
YATES JRW
BARTON DE
Citation: Dj. Dow et al., INSTABILITY OF A NORMAL (CTG), ALLELE IN THE DM-KINASE GENE, Journal of Medical Genetics, 32(2), 1995, pp. 151-151
Authors:
JOYCE JA
FROGGATT NJ
DAVIES R
EVANS DGR
TREMBATH R
BARTON DE
MAHER ER
Citation: Ja. Joyce et al., MOLECULAR-GENETIC ANALYSIS OF EXON-1 TO EXON-6 OF THE APC GENE IN NONPOLYPOSIS FAMILIAL COLORECTAL-CANCER, Clinical genetics, 48(6), 1995, pp. 299-303
Authors:
RUBINSZTEIN DC
BARTON DE
FERGUSONSMITH MA
Citation: Dc. Rubinsztein et al., ISSUES IN HUNTINGTONS-DISEASE TESTING, Quarterly Journal of Medicine, 87(2), 1994, pp. 71-73
Authors:
RUBINSZTEIN DC
AMOS W
LEGGO J
GOODBURN S
RAMESAR RS
OLD J
BONTROP R
MCMAHON R
BARTON DE
FERGUSONSMITH MA
Citation: Dc. Rubinsztein et al., MUTATIONAL BIAS PROVIDES A MODEL FOR THE EVOLUTION OF HUNTINGTONS-DISEASE AND PREDICTS A GENERAL INCREASE IN DISEASE PREVALENCE, Nature genetics, 7(4), 1994, pp. 525-530
Authors:
MCMAHON R
MULLIGAN LM
HEALEY CS
PAYNE SJ
PONDER M
FERGUSONSMITH MA
BARTON DE
PONDER BAJ
Citation: R. Mcmahon et al., DIRECT, NONRADIOACTIVE DETECTION OF MUTATIONS IN MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A FAMILIES, Human molecular genetics, 3(4), 1994, pp. 643-646
Authors:
IRVING RM
MOFFAT DA
HARDY DG
BARTON DE
XUEREB JH
MAHER ER
Citation: Rm. Irving et al., SOMATIC NF2 GENE-MUTATIONS IN FAMILIAL AND NONFAMILIAL VESTIBULAR SCHWANNOMA, Human molecular genetics, 3(2), 1994, pp. 347-350
Authors:
RUBINSZTEIN DC
LEGGO J
AMOS W
BARTON DE
FERGUSONSMITH MA
Citation: Dc. Rubinsztein et al., MYOTONIC-DYSTROPHY CTG REPEATS AND THE ASSOCIATED INSERTION DELETION POLYMORPHISM IN HUMAN AND PRIMATE POPULATIONS/, Human molecular genetics, 3(11), 1994, pp. 2031-2035