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    1. Stewart, A; Haites, N; Rose, P
      Online medical genetics resources: a UK perspective

      BRITISH MEDICAL JOURNAL
    2. Haites, N; Miedzybrodzka, Z; Dean, J
      Stored tissue may be important for the future care of families

      BRITISH MEDICAL JOURNAL
    3. Cumming, GP; Narayansingh, GV; Parkin, DE; Haites, N
      Sequential occurrence within three years in a premenopausal woman of cervical, ovarian, and endometrial cancers - Drug induced long QT syndrome.

      POSTGRADUATE MEDICAL JOURNAL
    4. Stewart, K; Wilson, P; Wilson, H; Minto, A; Haites, N; Whiting, P; Macleod, A; Brown, P
      Thy1 glomerulonephritis induced in young Lewis rats accelerates age-related glomerulosclerosis

      NEPHRON
    5. Stewart, GS; Last, JIK; Stankovic, T; Haites, N; Kidd, AMJ; Byrd, PJ; Taylor, AMR
      Residual ataxia telangiectasia mutated protein function in cells from ataxia telangiectasia patients, with 5762ins137 and 7271T -> G mutations, showing a less severe phenotype

      JOURNAL OF BIOLOGICAL CHEMISTRY
    6. Semple, S; Dick, F; Osborne, A; Cherrie, JW; Soutar, A; Seaton, A; Haites, N
      Impairment of colour vision in workers exposed to organic solvents

      OCCUPATIONAL AND ENVIRONMENTAL MEDICINE
    7. Lakhani, SR; Gusterson, BA; Jacquemier, J; Sloane, JP; Anderson, TJ; van de Vijver, MJ; Venter, D; Freeman, A; Antoniou, A; McGuffog, L; Smyth, E; Steel, CM; Haites, N; Scott, RJ; Goldgar, D; Neuhausen, S; Daly, PA; Ormiston, W; McManus, R; Scherneck, S; Ponder, BAJ; Futreal, PA; Peto, J; Stoppa-Lyonnet, D; Bignon, YJ; Struewing, JP; Bishop, DT; Klijn, JGM; Devilee, P; Cornelisse, CJ; Lasset, C; Lenoir, G; Barkardottir, RB; Egilsson, V; Hamann, U; Chang-Claude, J; Sobol, H; Weber, B; Easton, DF; Stratton, MR
      The pathology of familial breast cancer: Histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2

      CLINICAL CANCER RESEARCH
    8. Vigen, T; Haites, N; Burn, J; Moller, P; Steel, M
      Patenting genes: a dangerous EU directive

      BRITISH JOURNAL OF GENERAL PRACTICE
    9. Donaghy, M; Sisodiya, SM; Kennett, R; McDonald, B; Haites, N; Bell, C
      Steroid responsive polyneuropathy in a family with a novel myelin protein zero mutation

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    10. Murray, TJ; Fowler, PA; Abramovich, DR; Haites, N; Lea, RG
      Human fetal testis: Second trimester proliferative and steroidogenic capacities

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    11. Nelis, E; Haites, N; Van Broeckhoven, C
      Mutations in the peripheral myelin genes and associated genes in inheritedperipheral neuropathies

      HUMAN MUTATION
    12. Miedzybrodzka, Z; Hattersley, AT; Ellard, S; Pearson, D; de Silva, D; Harvey, R; Haites, N
      Non-penetrance in a MODY 3 family with a mutation in the hepatic nuclear factor 1 alpha gene: implications for predictive testing

      EUROPEAN JOURNAL OF HUMAN GENETICS
    13. Haites, N; Brown, I; Milner, B; Steel, M
      Untitled

      DISEASE MARKERS
    14. Hodgson, S; Milner, B; Brown, I; Bevilacqua, G; Chang-Claude, J; Eccles, D; Evans, G; Gregory, H; Moller, P; Morrison, P; Steel, M; Stoppa-Lyonnet, D; Vasen, H; Haites, N
      Cancer genetics services in Europe

      DISEASE MARKERS
    15. Chang-Claude, J; Becher, H; Caligo, M; Eccles, D; Evans, G; Haites, N; Hodgson, S; Moller, P; Weber, BHF; Stoppa-Lyonnet, D
      Risk estimation as a decision-making tool for genetic analysis of the breast cancer susceptibility genes

      DISEASE MARKERS
    16. Steel, M; Smyth, E; Vasen, H; Eccles, D; Evans, G; Moller, P; Hodgson, S; Stoppa-Lyonnet, D; Chang-Claude, J; Caligo, M; Morrison, P; Haites, N
      Ethical, social and economic issues in familial breast cancer: a compilation of views from the EC biomed II demonstration project

      DISEASE MARKERS
    17. Evans, DGR; Anderson, E; Lalloo, F; Vasen, H; Beckmann, M; Eccles, D; Hodgson, S; Moller, P; Chang-Claude, J; Morrison, P; Stoppa-Lyonnet, D; Steel, M; Haites, N
      Utilisation of prophylactic mastectomy in 10 European centers

      DISEASE MARKERS
    18. Miedzybrodzka, Z; Hamilton, NM; Gregory, H; Milner, B; Frade, I; Sinclair, T; Mollison, J; Haites, N
      Teaching breast cancer genetics to medical students: Evaluation of a computer assister learning (CAL) package

      DISEASE MARKERS
    19. Moller, P; Reis, MM; Evans, G; Vasen, H; Haites, N; Anderson, E; Steel, CM; Apold, J; Lalloo, F; Maehle, L; Preece, P; Gregory, H; Heimdal, K
      Efficacy of early diagnosis and treatment in women with a family history of breast cancer

      DISEASE MARKERS
    20. Eccles, DM; Simmonds, P; Goddard, J; Coultas, M; Lalloo, F; Evans, G; Haites, N
      Management of hereditary breast cancer

      DISEASE MARKERS
    21. Gregory, H; Gibbons, B; Haites, N
      Audit of women attending the Aberdeen Genetic Clinic with a family historyof breast cancer who subsequently develop cancer

      DISEASE MARKERS
    22. Moller, P; Borg, A; Evans, G; Haites, N; Steel, CM; Vasen, H; Gregory, H; Hodgson, S; Apold, J; Lalloo, F; Maehle, L; Anderson, E; Heimdal, K
      Mutation-specific survival of inherited breast cancer

      DISEASE MARKERS
    23. Moller, P; Evans, G; Haites, N; Vasen, H; Reis, MM; Anderson, E; Apold, J; Hodgson, S; Eccles, D; Olsson, H; Stoppa-Lyonnet, D; Chang-Claude, J; Morrison, PJ; Bevilacqua, G; Heimdal, K; Maehle, L; Lalloo, F; Gregory, H; Preece, P; Borg, A; Nevin, NC; Caligo, M; Steel, CM
      Guidelines for follow-up of women at high risk for inherited breast cancer: Consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer

      DISEASE MARKERS
    24. Miedzybrodzka, Z; Loughlin, S; Baty, D; Terron, A; Kelly, K; Dean, J; Greaves, M; Pippard, M; Haites, N
      Haemochromatosis mutations in North-East Scotland

      BRITISH JOURNAL OF HAEMATOLOGY
    25. Burn, J; Alonso, A; Bertario, L; Bishop, T; Bisgaard, ML; Cummings, J; Davidson, R; Delhanty, J; Demant, P; Dunlop, M; Eccles, D; Ellis, A; Evans, G; Fidalgo, P; Fodde, R; Haites, N; Hodgson, S; Hultcrantz, R; Huson, S; Jarvinen, H; Kartheuser, A; Kleibeuker, J; Lenaerts, C; Lucasson, A; Lunt, P; McDermot, K; McKay, J; McKeown, C; Maher, E; Mathers, J; Mecklin, JP; Moslein, G; Murday, V; Nagengast, F; Northover, JMA; Obrador, A; Parks, TG; Paraskeva, C; Phillips, R; San Roman, C; Ruscheoff, J; Sampson, J; Shepherd, N; Tempesta, A; Trembath, R; Turnpenny, P; Vasen, HFA
      Concerted action polyp prevention, CAPP2: A trial of aspirin and/or resistant starch in people at risk of hereditary non-polyposis colon cancer (HNPCC)

      CANCER RESEARCH SUPPORTED UNDER BIOMED I
    26. Devilee, P; Barkardottir, RB; Bevilacqua, G; Bignon, YJ; Bishop, T; Borg, A; Borresen-Dale, AL; Chang-Claude, J; Easton, D; Eyfjord, J; Feunteun, J; Goldgar, D; Haites, N; Holm, N; Kruse, T; Larsson, C; Lenoir, G; Lidereau, R; Nevanlinna, H; Ponder, B; Scherneck, S; Schmitt, F; Sobol, H; Solomon, E; Spurr, N; Steel, M; Stratton, M; Varley, J; Vasen, H; Vassilaros, S; Wagner, T; Willems, P; Winqvist, R
      Genetics and epidemiology of hereditary breast cancer

      CANCER RESEARCH SUPPORTED UNDER BIOMED I
    27. MIEDZYBRODZKA Z; LOUGHLIN S; BATY D; TERRON A; KELLY K; HAITES N; DEAN J; GOUDIE D; GREAVES M
      THE GENETIC COMPLEXITY OF HEMOCHROMATOSIS IN NE SCOTLAND

      British Journal of Haematology
    28. BELL C; HAITES N
      GENETIC-ASPECTS OF CHARCOT-MARIE-TOOTH DISEASE

      Archives of Disease in Childhood
    29. FORD D; EASTON DF; STRATTON M; NAROD S; GOLDGAR D; DEVILEE P; BISHOP DT; WEBER B; LENOIR G; CHANGCLAUDE J; SOBOL H; TEARE MD; STRUEWING J; ARASON A; SCHERNECK S; PETO J; REBBECK TR; TONIN P; NEUHAUSEN S; BARKARDOTTIR R; EYFJORD J; LYNCH H; PONDER BAJ; GAYTHER SA; BIRCH JM; LINDBLOM A; STOPPALYONNET D; BIGNON Y; BORG A; HAMANN U; HAITES N; SCOTT RJ; MAUGARD CM; VASEN H
      GENETIC-HETEROGENEITY AND PENETRANCE ANALYSIS OF THE BRCA1 AND BRCA2 GENES IN BREAST-CANCER FAMILIES

      American journal of human genetics
    30. STANKOVIC T; KIDD AMJ; SUTCLIFFE A; MCGUIRE GM; ROBINSON P; WEBER P; BEDENHAM T; BRADWELL AR; EASTON DF; LENNOX GG; HAITES N; BYRD PJ; TAYLOR AMR
      ATM MUTATIONS AND PHENOTYPES IN ATAXIA-TELANGIECTASIA FAMILIES IN THEBRITISH-ISLES - EXPRESSION OF MUTANT ATM AND THE RISK OF LEUKEMIA, LYMPHOMA, AND BREAST-CANCER

      American journal of human genetics
    31. LAKHANI SR; JACQUEMIER J; SLOANE JP; GUSTERSON BA; ANDERSON TJ; VANDEVIJVER MJ; FARID LM; VENTER D; ANTONIOU A; STORFERISSER A; SMYTH E; STEEL CM; HAITES N; SCOTT RJ; GOLDGAR D; NEUHAUSEN S; DALY PA; ORMISTON W; MCMANUS R; SCHERNECK S; PONDER BAJ; FORD D; PETO J; STOPPALYONNET D; BIGNON YJ; STRUEWING JP; SPURR NK; BISHOP DT; KLIJN JGM; DEVILEE P; CORNELISSE CJ; LASSET C; LENOIR G; BARKARDOTTIR RB; EGILSSON V; HAMANN U; CHANGCLAUDE J; SOBOL H; WEBER B; STRATTON MR; EASTON DF
      MULTIFACTORIAL ANALYSIS OF DIFFERENCES BETWEEN SPORADIC BREAST CANCERS AND CANCERS INVOLVING BRCA1 AND BRCA2 MUTATIONS

      Journal of the National Cancer Institute
    32. MULLER HW; SUTER U; VANBROECKHOVEN C; HANEMAN O; NELIS E; TIMMERMAN V; SANCHO S; BARRIO L; BOLHUIS P; DERMIETZEL R; FRANK M; GABREELSFESTEN A; GILLEN C; HAITES N; LEVI G; MARIMAN E; MARTINI R; NAVE K; RAUTENSTRAUSS B; SCHACHNER M; SCHENONE A; SCHNEIDER C; SCHRODER M; WILLECKE K
      ADVANCES IN CHARCOT-MARIE-TOOTH-DISEASE RESEARCH - CELLULAR FUNCTION OF CMT-RELATED PROTEINS, TRANSGENIC ANIMAL-MODELS, AND PATHOMECHANISMS

      Neurobiology of disease
    33. LAKHANI SR; EASTON DF; STRATTON MR; STORFERISSER A; ANDERSON TJ; FARID LM; GUSTERSON BA; JAQUEMIER J; SLOANE JP; VENTER D; VANDEVIJVER MJ; BISHOP DT; BARKARDOTTIR RB; BIGNON YJ; CORNELISSE C; CHANGCLAUDE J; DALY PA; DEVILEE P; EGILSSON V; FORD D; GOLDGAR D; HAITES N; HAMANN U; KLIJN JGM; LASSET C; LENOIR G; MCMANUS R; NEUHAUSEN S; ORMISTON W; PONDER BAJ; PETO J; STEEL CM; STOPPALYONNET D; SMYTH E; SOBOL H; SPURR NK; SCOTT RJ; SCHERNECK S; STREUWING JP; VASEN H; WEBER B
      PATHOLOGY OF FAMILIAL BREAST-CANCER - DIFFERENCES BETWEEN BREAST CANCERS IN CARRIERS OF BRCA1 OR BRCA2 MUTATIONS AND SPORADIC CASES

      Lancet
    34. GREGORY H; PEARSON R; MCLEOD A; SCHOFIELD A; HAITES N; GILBERT F
      COMPARISON OF MAMMOGRAPHIC APPEARANCES IN BRCA1 CARRIERS AND NONCARRIERS IN A FAMILY WITH A 1294DE140 MUTATION

      Journal of Medical Genetics
    35. GREGORY H; VASEN H; MILNER B; HAITES N
      BIOMED-2 DEMONSTRATION PROJECT - EVALUATION OF CURRENT SURVEILLANCE AND MANAGEMENT OF PATIENTS AT HIGH-RISK OF BREAST-CANCER IN WESTERN-EUROPE

      Journal of Medical Genetics
    36. MIEDZYBRODZKA Z; HAITES N; PEARSON D; HATTERSLEY A; DESILVA D
      CLINICAL PHENOTYPE IN A MODY-3 FAMILY WITH A MISSENSE MUTATION IN THEHEPATIC NUCLEAR FACTOR-1 GENE

      Journal of Medical Genetics
    37. KIDD A; DEAN J; HAITES N
      CASE-REPORT OF A PATIENT WITH ACROMEGALOID APPEARANCE, CONGENITAL HYPERTRICHOSIS AND A HISTORY OF PERICARDIAL-EFFUSIONS

      Journal of Medical Genetics
    38. LOUGHLIN S; MIEDZYBRODZKA Z; BATY D; TERRON A; KELLY K; DEAN J; GOUDIE D; GREAVES M; HAITES N
      HEMOCHROMATOSIS MUTATIONS IN NORTHEAST SCOTLAND

      Journal of Medical Genetics
    39. STANKOVIC T; BYRD PJ; KIDD AMJ; SUTCLIFFE A; MCGUIRE GM; ROBINSON P; WEBER P; BEDENHAM T; EASTON DF; LENNOX GG; HAITES N; TAYLOR AMR
      ATM MUTATIONS AND PHENOTYPES IN A-T FAMILIES IN THE BRITISH-ISLES - EXPRESSION OF MUTANT ATM AND THE RISK OF LEUKEMIA, LYMPHOMA AND BREAST-CANCER

      American journal of human genetics
    40. TONKIN ET; MOHAMED Z; HAITES N; SHAW DJ
      IDENTIFICATION OF CANDIDATE GENES FOR AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA (RP10) MAPPING TO 7Q31-Q35

      American journal of human genetics
    41. WICKING C; SHANLEY S; SMYTH I; GILLIES S; NEGUS K; GRAHAM S; SUTHERS G; HAITES N; EDWARDS M; WAINWRIGHT B; CHENEVIXTRENCH G
      MOST GERM-LINE MUTATIONS IN THE NEVOID BASAL-CELL CARCINOMA SYNDROME LEAD TO A PREMATURE TERMINATION OF THE PATCHED PROTEIN, AND NO GENOTYPE-PHENOTYPE CORRELATIONS ARE EVIDENT

      American journal of human genetics
    42. DESILVA D; HAITES N; WALTER LG
      PSYCHOLOGICAL EFFECTS OF INDIVIDUALIZED BREAST-CANCER RISK COUNSELING

      Psycho-oncology
    43. DUTHIE L; HILLIS G; SIMPSON J; HAITES N; MACLEOD A
      CONNEXIN-43 EXPRESSION IN RAPIDLY PROGRESSIVE GLOMERULONEPHRITIS

      Journal of the American Society of Nephrology
    44. SCHOFIELD A; MUIR E; DESILVA D; GREGORY H; HAITES N
      MALE BREAST-CANCER - THE IMPORTANCE OF RECOGNIZING FAMILY HISTORY ANDTHE PRELIMINARY-RESULTS OF LINKAGE ANALYSIS TO BRCA1 AND BRCA2

      Breast
    45. KIDD A; CARSON L; GREGORY DW; DESILVA D; HOLMES J; DEAN JCS; HAITES N
      A SCOTTISH FAMILY WITH BAZEX-DUPRE-CHRISTOL SYNDROME - FOLLICULAR ATROPHODERMA, CONGENITAL HYPOTRICHOSIS, AND BASAL-CELL CARCINOMA

      Journal of Medical Genetics
    46. GREGORY H; SCHOFIELD A; DESILVA D; SEMPER J; MILNER B; ALLAN L; HAITES N
      ASCERTAINMENT OF FAMILIAL OVARIAN-CANCER IN THE ABERDEEN-GENETIC-CLINIC

      Journal of Medical Genetics
    47. HAITES N; BELL C; COCHRANE S; FAIRWEATHER N; MONACO T; JOHNSTON A
      CONNEXIN-32 MUTATIONS IN X-LINKED DOMINANT CHARCOT-MARIE-TOOTH-DISEASE

      Journal of Medical Genetics
    48. GATES LJ; MACCONNACHIE A; BENJAMIN N; HAITES N
      DESCRIPTION OF 2 FAMILIES IN THE NORTH-EAST OF SCOTLAND WITH GLUCOCORTICOID-REMEDIABLE ALDOSTERONISM

      Journal of Medical Genetics
    49. KIDD A; TURNPENNY P; KELLY K; CLARK C; CHURCH W; HUTCHINSON C; DEAN J; HAITES N
      ASCERTAINMENT OF MYOTONIC-DYSTROPHY THROUGH CATARACT BY SELECTIVE SCREENING

      Journal of Medical Genetics
    50. SCHOFIELD A; MILNER B; ALLAN L; HAITES N
      USE OF LINKED MARKERS IN BREAST OVARIAN CANCER FAMILIES/

      Journal of Medical Genetics
    51. DESILVA D; STEVENSON D; GRAY E; DEAN J; DUNLOP M; HAITES N
      CRANIAL DESMOID TUMOR AS THE FIRST PRESENTATION OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP) AND THE DEMONSTRATION OF THE ROLE OF THE APC GENE IN THE PATHOGENESIS OF THIS TUMOR

      Journal of Medical Genetics
    52. DESILVA D; GILBERT F; NEEDHAM G; DEANS H; TUMPENNY P; HAITES N
      IDENTIFICATION OF WOMEN AT HIGH GENETIC RISK OF BREAST-CANCER THROUGHTHE NATIONAL-HEALTH-SERVICE BREAST SCREENING-PROGRAM (NHSBSP)

      Journal of Medical Genetics
    53. NAROD SA; FORD D; DEVILEE P; BARKARDOTTIR RB; LYNCH HT; SMITH SA; PONDER BAJ; WEBER BL; GARBER JE; BIRCH JM; CORNELIS RS; KELSELL DP; SPURR NK; SMYTH E; HAITES N; SOBOL H; BIGNON YJ; CHANGCLAUDE J; HAMANN U; LINDBLOM A; BORG A; PIVER MS; GALLION HH; STRUEWING JP; WHITTEMORE A; TONIN P; GOLDGAR DE; EASTON DF; MILNER B; ALLAN L; SIMARD J; ROMMENS J; MCGILLIVRAY B; GREEN R; IVES E; BOYD N; ROSEN B; COLE D; MORGAN K; MOSLEHI R; PONDER B; PETO J; SMITH S; STRATTON M; DICIOCCIO RA; GALLION H; SANTIBANEZKOREF MS; TEARE MD; EVANS DG; STOPPALYONNET D; LALLE P; BONAITI C; ESSIOUX L; GIRODET C; MAUGARDLOUBOUTIN C; NICOLLEAU G; LONGY M; TOULOUSE C; HORSTEIN I; BIRNBAUM D; EISINGER F; KARENGUEVEN F; NOGUCHI T; HARDOUIN A; RIO P; MACHELARDROUMAGNAC M; NOGUES C; COHENHAGUENAUER O; LORTHOLARY A; BAY JO; ARASON A; BARKDARDOTTIR RB; EGILSSON V; BISHOP DT; KELSELL D; MURDAY VA; SOLOMON E; SPURR N; TURNER G; LENOIR G; FEUNTEUN J; LYNCH H; LYNCH J; WATSON P; CONWAY T; BONNARDEL C; SEROVA O; TORCHARD D; LARSSON C; VASEN H; VANLEEUWEN I; CORNELISSE CJ; STEEL M; PORTER D; COHEN BB; CAROTHERS A; CANNONALBRIGHT LA; GOLDGAR D; SKOLNICK M; BECHER H; JOHANNSSON O; WEBER B; COLLINS F; BOEHNKE M; GARBER J; LI F
      AN EVALUATION OF GENETIC-HETEROGENEITY IN 145 BREAST-CANCER OVARIAN-CANCER FAMILIES

      American journal of human genetics
    54. EASTON DF; FORD D; BISHOP DT; HAITES N; MILNER B; ALLAN L; EASTON DF; PONDER BAJ; PETO J; SMITH S; FORD D; STRATTON M; NAROD SA; LENOIR GM; FEUNTEUN J; LYNCH H; ARASON A; BARKDARDOTTIR R; EGILSSON DV; BISHOP DT; BLACK DM; KELSELL D; SPURR NK; DEVILEE P; CORNELISSE CJ; VARSEN H; BIRCH JM; SANTIBANEZKOREF MS; TEARE MD; STEEL M; PORTER D; COHEN BB; CAROTHERS A; SMYTH E; WEBER B; BOEHNKE M; COLLINS FS; CANNONALBRIGHT LA; GOLDGAR D; SKOLNICK M
      BREAST AND OVARIAN-CANCER INCIDENCE IN BRCAI-MUTATION CARRIERS

      American journal of human genetics
    55. PERICAKVANCE MA; BARKER DF; BERGOFFEN JA; CHANCE P; COCHRANE S; DAHL N; EXLER MC; FAIN PR; FAIRWEATHER ND; FISCHBECK K; GAL A; HAITES N; IONASESCU R; IONASESCU VV; KENNERSON ML; MONACO AP; MOSTACCUIOLO M; NICHOLSON GA; SILLEN A; HAINES JL
      CONSORTIUM FINE LOCALIZATION OF X-LINKED CHARCOT-MARIE-TOOTH DISEASE (CMTX1) - ADDITIONAL SUPPORT THAT CONNEXIN32 IS THE DEFECT IN CMTX1

      Human heredity
    56. FORD D; EASTON DF; BISHOP DT; NAROD SA; GOLDGAR DE; HAITES N; MILNER B; ALLAN L; PONDER BAJ; PETO J; SMITH S; STRATTON M; LENOIR GM; FEUNTEUN J; LYNCH H; ARASON A; BARKARDOTTIR R; EGILSSON V; BLACK DM; KELSELL D; SPURR N; DEVILEE P; CORNELISSE CJ; VARSEN H; BIRCH JM; SKOLNICK M; SANTIBANEZKOREF MS; TEARE D; STEEL M; PORTER D; COHEN BB; CAROTHERS A; SMYTH E; WEBER B; NEWBOLD B; BOEHNKE M; COLLINS FS; CANNONALBRIGHT LA; GOLDGAR D
      RISKS OF CANCER IN BRCA1-MUTATION CARRIERS

      Lancet
    57. MIEDZYBRODZKA Z; TEMPLETON A; DEAN J; HAITES N; MOLLISON J; SMITH N
      PREIMPLANTATION DIAGNOSIS OR CHORIONIC VILLUS BIOPSY - WOMENS ATTITUDES AND PREFERENCES

      Human reproduction
    58. MIEDZYBRODZKA Z; HAITES N; DEAN J
      APPROACHES TO PRENATAL CYSTIC-FIBROSIS CARRIER SCREENING - REPLY

      Journal of Medical Genetics
    59. BERGOFFEN J; CHEN K; NIEUWENHUIJSEN BW; COCHRANE S; FAIRWEATHER N; MONACO A; HAITES N; FISCHBECK KH
      LOCALIZATION OF X-LINKED CHARCOT-MARIE-TOOTH DISEASE TO XQ13.1

      American journal of human genetics
    60. MILNER BJ; ALLAN LA; KELLY KF; CRUICKSHANK D; HALL M; JOHNSTON A; KITCHENER H; PARKIN D; HAITES N
      LINKAGE STUDIES WITH 17Q AND 18Q MARKERS IN A BREAST OVARIAN-CANCER FAMILY

      American journal of human genetics


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Documento generato il 31/10/20 alle ore 03:45:26