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    1. Khoo, SK; Bradley, M; Wong, FK; Hedblad, MA; Nordenskjold, M; Teh, BT
      Birt-Hogg-Dube syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2

      ONCOGENE
    2. Nordgren, A; Farnebo, F; Johansson, B; Holmgren, G; Forestier, E; Larsson, C; Soderhall, S; Nordenskjold, M; Blennow, E
      Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping

      EUROPEAN JOURNAL OF HAEMATOLOGY
    3. Lindvall, C; Nordenskjold, M; Porwit, A; Bjorkholm, M; Blennow, E
      Molecular cytogenetic characterization of acute myeloid leukemia and myelodysplastic syndromes with multiple chromosome rearrangements

      HAEMATOLOGICA
    4. Grigelioniene, G; Schoumans, J; Neumeyer, L; Ivarsson, SA; Eklof, O; Enkvist, O; Tordai, P; Fosdal, I; Myhre, AG; Westphal, O; Nilsson, NO; Elfving, M; Ellis, I; Anderlid, BM; Fransson, I; Tapia-Paez, I; Nordenskjold, M; Hagenas, L; Dumanski, JP
      Analysis of short stature homeobox-containing gene (SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity

      HUMAN GENETICS
    5. Soderhall, C; Bradley, M; Kockum, I; Wahlgren, CF; Luthman, H; Nordenskjold, M
      Linkage and association to candidate regions in Swedish atopic dermatitis families

      HUMAN GENETICS
    6. Fridstrom, M; Ahrlund-Richter, L; Iwarsson, E; Malmgren, H; Inzunza, J; Rosenlund, B; Sjoblom, P; Nordenskjold, M; Blennow, E; Hovatta, O
      Clinical outcome of treatment cycles using preimplantation genetic diagnosis for structural chromosomal abnormalities

      PRENATAL DIAGNOSIS
    7. Nordgren, A; Schoumans, J; Soderhall, S; Nordenskjold, M; Blennow, E
      Interphase fluorescence in situ hybridization and spectral karyotyping reveals hidden genetic aberrations in children with acute lymphoblastic leukaemia and a normal banded karyotype

      BRITISH JOURNAL OF HAEMATOLOGY
    8. Ericson, KG; Fadeel, B; Nilsson-Ardnor, S; Soderhall, C; Samuelsson, A; Janka, G; Schneider, M; Gurgey, A; Yalman, N; Revesz, T; Egeler, RM; Jahnukainen, K; Storm-Mathiesen, I; Haraldsson, A; Poole, J; de Saint Basile, G; Nordenskjold, M; Henter, JI
      Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis

      AMERICAN JOURNAL OF HUMAN GENETICS
    9. Lindblom, A; Nordenskjold, M
      The biology of inherited cancer

      SEMINARS IN CANCER BIOLOGY
    10. Wong, FK; Burgess, J; Nordenskjold, M; Larsson, C; Teh, BT
      Multiple endocrine neoplasia type 1

      SEMINARS IN CANCER BIOLOGY
    11. Iwarsson, E; Malmgren, H; Inzunza, J; Ahrlund-Richter, L; Sjoblom, P; Rosenlund, B; Fridstrom, M; Hovatta, O; Nordenskjold, M; Blennow, E
      Highly abnormal cleavage divisions in preimplantation embryos from translocation carriers

      PRENATAL DIAGNOSIS
    12. Bjorck, EJ; Bui, TH; Wijmenga, C; Grandell, U; Nordenskjold, M
      Early prenatal diagnosis of the ICF syndrome

      PRENATAL DIAGNOSIS
    13. Zhang, AJ; Zheng, CY; Lindvall, C; Hou, M; Ekedahl, J; Lewensohn, R; Yan, ZQ; Yang, XY; Henriksson, M; Blennow, E; Nordenskjold, M; Zetterberg, A; Bjorkholm, M; Gruber, A; Xu, DW
      Frequent amplification of the Telomerase Reverse Transcriptase gene in human tumors

      CANCER RESEARCH
    14. Bradley, M; Kockum, I; Soderhall, C; van Hage-Hamsten, M; Luthman, H; Nordenskjold, M; Wahlgren, CF
      Characterization by phenotype of families with atopic dermatitis

      ACTA DERMATO-VENEREOLOGICA
    15. Li, CD; Berx, G; Larsson, C; Auer, G; Aspenblad, U; Pan, Y; Sundelin, B; Ekman, P; Nordenskjold, M; van Roy, F; Bergerheim, USR
      Distinct deleted regions on chromosome segment 16q23-24 associated with metastases in prostate cancer

      GENES CHROMOSOMES & CANCER
    16. Iwarsson, E; Lundqvist, M; Inzunza, J; Ahrlund-Richter, L; Sjoblom, P; Lundkvist, O; Simberg, N; Nordenskjold, M; Blennow, E
      A high degree of aneuploidy in frozen-thawed human preimplantation embryos

      HUMAN GENETICS
    17. Lindblom, A; Nordenskjold, M
      Hereditary cancer

      ACTA ONCOLOGICA
    18. Teh, BT; Larsson, C; Nordenskjold, M
      Tumor suppressor genes (TSG)

      ANTICANCER RESEARCH
    19. Carlson, KM; Gruber, A; Liliemark, E; Larsson, R; Nordenskjold, M
      Characterization of drug-resistant cell lines by comparative genomic hybridization

      CANCER GENETICS AND CYTOGENETICS
    20. Vorechovsky, I; Blennow, E; Nordenskjold, M; Webster, ADB; Hammarstrom, L
      A putative susceptibility locus on chromosome 18 is not a major contributor to human selective IgA deficiency: Evidence from meiotic mapping of 83 multiple-case families

      JOURNAL OF IMMUNOLOGY
    21. IWARSSON E; AHRLUNDRICHTER L; INZUNZA J; FRIDSTROM M; ROSENLUND B; HILLENSJO T; SJOBLOM P; NORDENSKJOLD M; BLENNOW E
      PREIMPLANTATION GENETIC DIAGNOSIS OF DIGEORGE-SYNDROME

      Molecular human reproduction (Print)
    22. IWARSSON E; AHRLUNDRICHTER L; INZUNZA J; ROSENLUND B; FRIDSTROM M; HILLENSJO T; SJOBLOM P; NORDENSKJOLD M; BLENNOW E
      PREIMPLANTATION GENETIC DIAGNOSIS OF A LARGE PERICENTRIC-INVERSION OFCHROMOSOME-5

      Molecular human reproduction (Print)
    23. LI CD; WEBER G; EKMAN P; LAGERCRANTZ J; NORLEN BJ; AKERSTROM G; NORDENSKJOLD M; BERGERHEIM USR
      GERMLINE MUTATIONS DETECTED IN THE VON-HIPPEL-LINDAU DISEASE TUMOR-SUPPRESSOR GENE BY SOUTHERN BLOT AND DIRECT GENOMIC DNA-SEQUENCING

      Human mutation
    24. IWARSSON E; LUNDQUIST M; INZUNZA J; AHRLUNDRICHTER L; NORDENSKJOLD M; SJOBLOM P; LUNDKVIST O; SIMBERG N; BLENNOW E
      NUMERICAL CHROMOSOMAL-ABNORMALITIES IN TRIPRONUCLEAR PREIMPLANTATION EMBRYOS FERTILIZED IN-VITRO

      Human reproduction (Oxford. Print)
    25. IWARSSON E; AHRLUNDRICHTER L; INZUNZA J; ROSENLUND B; FRIDSTROM M; SJOBLOM P; NORDENSKJOLD M; BLENNOW E
      BIRTH OF HEALTHY TWINS AFTER PREIMPLANTATION GENETIC DIAGNOSIS OF A PERICENTRIC-INVERSION OF CHROMOSOME-5

      Human reproduction (Oxford. Print)
    26. Inzunza, J; Iwarsson, E; Fridstrom, M; Rosenlund, B; Sjoblom, P; Hillensjo, T; Blennow, E; Jones, B; Nordenskjold, M; Ahrlund-Richter, L
      Application of single-needle blastomere biopsy in human preimplantation genetic diagnosis

      PRENATAL DIAGNOSIS
    27. TEH BT; KYTOLA S; FARNEBO F; BERGMAN L; WONG FK; WEBER G; HAYWARD N; LARSSON C; SKOGSEID B; BECKERS A; PHELAN C; EDWARDS M; EPSTEIN M; ALFORD F; HURLEY D; GRIMMOND S; SILINS G; WALTERS M; STEWART C; CARDINAL J; KHODAEI S; PARENTE F; TRANEBJAERG L; JORDE R; MENON J; KHIR A; TAN TT; CHAN SP; ZAINI A; KHALID BAK; SANDELIN K; THOMPSON N; BRANDI ML; WARTH M; STOCK J; LEISTI J; CAMERON D; SHEPHERD JJ; OBERG K; NORDENSKJOLD M; SALMELA P
      MUTATION ANALYSIS OF THE MEN1 GENE IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-1, FAMILIAL ACROMEGALY AND FAMILIAL ISOLATED HYPERPARATHYROIDISM

      The Journal of clinical endocrinology and metabolism
    28. TEH BT; ESAPA CT; HOULSTON R; GRANDELL U; FARNEBO F; NORDENSKJOLD M; PEARCE CJ; CARMICHAEL D; LARSSON C; HARRIS PE
      A FAMILY WITH ISOLATED HYPERPARATHYROIDISM SEGREGATING A MISSENSE MEN1 MUTATION AND SHOWING LOSS OF THE WILD-TYPE ALLELES IN THE PARATHYROID TUMORS

      American journal of human genetics
    29. CARLSON KM; BRUDER C; NORDENSKJOLD M; DUMANSKI JP
      1P AND 3P DELETIONS IN MENINGIOMAS WITHOUT DETECTABLE ABERRATIONS OR CHROMOSOME-22 IDENTIFIED BY COMPARATIVE GENOMIC HYBRIDIZATION

      Genes, chromosomes & cancer
    30. BAJALICALAGERCRANTZ S; PIEHL F; LAGERCRANTZ J; LINDAHL J; WEBER G; KERCKEART JP; PORWITMACDONALD A; NORDENSKJOLD M
      EXPRESSION OF LAZ3 BCL6 IN FOLLICULAR CENTER (FC) B-CELLS OF REACTIVELYMPH-NODES AND FC-DERIVED NON-HODGKIN LYMPHOMAS/

      Leukemia
    31. WEBER G; GRIMMOND S; LAGERCRANTZ J; FRIEDMAN E; PHELAN C; CARSON E; HAYWARD N; JACOBOVITZ O; NORDENSKJOLD M; LARSSON C
      EXCLUSION OF THE PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE C-BETA-3 (PLCB3) GENE AS A CANDIDATE FOR MULTIPLE ENDOCRINE NEOPLASIA TYPE-1

      Human genetics
    32. TANNERGARD P; LIU T; WEGER A; NORDENSKJOLD M; LINDBLOM A
      TUMORIGENESIS IN COLORECTAL TUMORS FROM PATIENTS WITH HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER

      Human genetics
    33. NORDGREN A; NORDENSKJOLD M; SODERHALL S; PORWITMACDONALD A; BLENNOW E
      A CASE OF ACUTE LYMPHOBLASTIC-LEUKEMIA, NEAR-TRIPLOIDY, AND POOR OUTCOME - CHARACTERIZATION BY FLUORESCENCE IN-SITU HYBRIDIZATION USING CHROMOSOME-SPECIFIC LIBRARIES FROM ALL HUMAN-CHROMOSOMES

      Cancer genetics and cytogenetics
    34. ENMARK E; PELTOHUIKKO M; GRANDIEN K; LAGERCRANTZ S; LAGERCRANTZ J; FRIED G; NORDENSKJOLD M; GUSTAFSSON JA
      HUMAN ESTROGEN-RECEPTOR BETA-GENE STRUCTURE, CHROMOSOMAL LOCALIZATION, AND EXPRESSION PATTERN

      The Journal of clinical endocrinology and metabolism
    35. GRIMMOND S; LAGERCRANTZ J; DRINKWATER C; SILINS G; TOWNSON S; POLLOCK P; GOTLEY D; CARSON E; RAKAR S; NORDENSKJOLD M; WARD L; HAYWARD N; WEBER G
      CLONING AND CHARACTERIZATION OF A NOVEL HUMAN GENE-RELATED TO VASCULAR ENDOTHELIAL GROWTH-FACTOR

      PCR methods and applications
    36. SZELES A; BAJALICALAGERCRANTZ S; LINDBLOM A; LUSHNIKOVA T; KASHUBA VI; IMREH S; NORDENSKJOLD M; KLEIN G; ZABAROVSKY ER
      MAPPING OF A NEW MAP KINASE ACTIVATED PROTEIN-KINASE GENE (3PK) TO HUMAN-CHROMOSOME BAND-3P21.2 AND ORDERING OF 3PK AND 2 COSMID MARKERS INTHE 3P22-P21 TUMOR-SUPPRESSOR REGION BY 2-COLOR FLUORESCENCE IN-SITU HYBRIDIZATION

      Chromosome research
    37. LAGERCRANTZ J; CARSON E; LARSSON C; NORDENSKJOLD M; WEBER G
      ISOLATION AND CHARACTERIZATION OF A NOVEL GENE CLOSE TO THE HUMAN PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE-C BETA-3 GENE ON CHROMOSOMAL REGION 11Q13

      Genomics
    38. DEMARCO L; STRATAKIS CA; BOSON WL; JAKBOVITZ O; CARSON E; ANDRADE LM; AMARAL VF; ROCHA JL; CHOURSOS GP; NORDENSKJOLD M; FRIEDMAN E
      SPORADIC CARDIAC MYXOMAS AND TUMORS FROM PATIENTS WITH CARNEY COMPLEXARE NOT ASSOCIATED WITH ACTIVATING MUTATIONS OF THE GS-ALPHA GENE

      Human genetics
    39. BAJALICALAGERCRANTZ S; PEDERSEN NT; SORENSEN AG; NORDENSKJOLD M
      DUPLICATION OF 2Q31-QTER AS A SOLE ABERRATION IN A CASE OF NON-HODGKINS-LYMPHOMA

      Cancer genetics and cytogenetics
    40. ENG C; CLAYTON D; SCHUFFENECKER I; LENOIR G; COTE G; GAGEL RF; VANAMSTEL HKP; LIPS CJM; NISHISHO I; TAKAI SI; MARSH DJ; ROBINSON BG; FRANKRAUE K; RAUE F; XUE FY; NOLL WW; ROMEI C; PACINI F; FINK M; NIEDERLE B; ZEDENIUS J; NORDENSKJOLD M; KOMMINOTH P; HENDY GN; GHARIB H; THIBODEAU SN; LACROIX A; FRILLING A; PONDER BAJ; MULLIGAN LM
      THE RELATIONSHIP BETWEEN SPECIFIC RET PROTOONCOGENE MUTATIONS AND DISEASE PHENOTYPE IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-2 - INTERNATIONAL RET MUTATION CONSORTIUM ANALYSIS

      JAMA, the journal of the American Medical Association
    41. LAGERCRANTZ J; KEDRA D; CARSON E; NORDENSKJOLD M; DUMANSKI JP; WEBER G; PIEHL F
      SEQUENCE AND EXPRESSION OF THE MOUSE HOMOLOG TO HUMAN PHOSPHOLIPASE-CBETA-3 NEIGHBORING GENE

      Biochemical and biophysical research communications
    42. TOWNSON S; LAGERCRANTZ J; GRIMMOND S; SILINS G; NORDENSKJOLD M; WEBER G; HAYWARD N
      CHARACTERIZATION OF THE MURINE VEGF-RELATED FACTOR GENE

      Biochemical and biophysical research communications
    43. TANNERGARD P; NORDENSKJOLD M; LINDBLOM A; LYSTROMLAHTI M; DELACHAPELLE A; PELTOMAKI P
      FINNISH MUTATIONS IN SWEDISH HNPCC FAMILIES (VOL 1, PG 1104, 1995)

      Nature medicine
    44. TANNERGARD P; NORDENSKJOLD M; LINDBLOM A
      FINNISH MUTATIONS IN SWEDISH HNPCC FAMILIES

      Nature medicine
    45. BAJALICA S; BRONDUMNIELSEN K; SORENSEN AG; PEDERSEN NT; KRISTOFFERSSON U; AKERMAN M; ANDERSON M; PISA P; NORDENSKJOLD M
      CHARACTERIZATION OF ADD(I)(P36) IN NON-HODGKIN LYMPHOMAS BY FLUORESCENCE IN-SITU HYBRIDIZATION

      Genes, chromosomes & cancer
    46. LAGERCRANTZ J; PIEHL F; NORDENSKJOLD M; LARSSON C; WEBER G
      EXPRESSION OF THE PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE C-BETA-3 GENE IN THE RAT

      NeuroReport
    47. NORDENSKJOLD M; HAMBERGER B; OBERG K
      MULTIPLE ENDOCRINE NEOPLASIA-1

      Journal of internal medicine
    48. LAGERCRANTZ J; LARSSON C; GRIMMOND S; SKOGSEID B; GOBL A; FRIEDMAN E; CARSON E; PHELAN C; OBERG K; NORDENSKJOLD M; HAYWARD NK; WEBER G
      CANDIDATE GENES FOR MULTIPLE ENDOCRINE NEOPLASIA TYPE-1

      Journal of internal medicine
    49. LAGERCRANTZ J; CARSON E; PHELAN C; GRIMMOND S; ROSEN A; DARE E; NORDENSKJOLD M; HAYWARD NK; LARSSON C; WEBER G
      GENOMIC ORGANIZATION AND COMPLETE CDNA SEQUENCE OF THE HUMAN PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE-C BETA-3 GENE (PLCB3)

      Genomics
    50. GRIMMOND S; WEBER G; LARSSON C; WALTERS M; TEH B; SHEPHERD J; NORDENSKJOLD M; HAYWARD N
      EXCLUSION OF THE 13-KDA RAPAMYCIN BINDING-PROTEIN GENE (FKBP2) AS A CANDIDATE GENE FOR MULTIPLE ENDOCRINE NEOPLASIA TYPE-1

      Human genetics
    51. AMARIGLIO N; FRIEDMAN E; MOR O; STIEBEL H; PHELAN C; COLLINS P; NORDENSKJOLD M; BROKSIMONI F; RECHAVI G
      ANALYSIS OF MICROSATELLITE REPEATS IN PEDIATRIC BRAIN-TUMORS

      Cancer genetics and cytogenetics
    52. BLENNOW E; NIELSEN KB; TELENIUS H; CARTER NP; KRISTOFFERSSON U; HOLMBERG E; GILLBERG C; NORDENSKJOLD M
      50 PROBANDS WITH EXTRA STRUCTURALLY ABNORMAL CHROMOSOMES CHARACTERIZED BY FLUORESCENCE IN-SITU HYBRIDIZATION

      American journal of medical genetics
    53. TANNERGARD P; LIPFORD JR; KOLODNER R; FRODIN JE; NORDENSKJOLD M; LINDBLOM A
      MUTATION SCREENING IN THE HMLH1 GENE IN SWEDISH HEREDITARY NONPOLYPOSIS COLON-CANCER FAMILIES

      Cancer research
    54. CARLSON K; BAJALICA S; NORDENSKJOLD M
      MOLECULAR CHARACTERIZATION OF DER(1)T(1-2)(P36-Q31) IN NON-HODGKIN LYMPHOMAS

      American journal of human genetics
    55. RUTTLEDGE MH; SARRAZIN J; RANGARATNAM S; PHELAN CM; TWIST E; MEREL P; DELATTRE O; THOMAS G; NORDENSKJOLD M; COLLINS VP; DUMANSKI JP; ROULEAU GA
      EVIDENCE FOR THE COMPLETE INACTIVATION OF THE NF2 GENE IN THE MAJORITY OF SPORADIC MENINGIOMAS

      Nature genetics
    56. RUTTLEDGE MH; XIE YG; HAN FY; PEYRARD M; COLLINS VP; NORDENSKJOLD M; DUMANSKI JP
      DELETIONS ON CHROMOSOME-22 IN SPORADIC MENINGIOMA

      Genes, chromosomes & cancer
    57. ZEDENIUS J; WALLIN G; HAMBERGER B; NORDENSKJOLD M; WEBER G; LARSSON C
      SOMATIC AND MEN 2A DE-NOVO MUTATIONS IDENTIFIED IN THE RET PROTOONCOGENE BY SCREENING OF SPORADIC MTC-S

      Human molecular genetics
    58. LARSSON C; NORDENSKJOLD M
      FAMILY SCREENING IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN-1)

      Annals of medicine
    59. LAGERCRANTZ J; WEBER G; FRIEDMAN E; GRIMMOND S; HAYWARD N; NORDENSKJOLD M; LARSSON C
      CANDIDATE GENES FOR MULTIPLE ENDOCRINE NEOPLASIA TYPE-1

      Journal of cellular biochemistry
    60. LINDBLOM A; TANNERGARD P; NORDENSKJOLD M
      DEFECTIVE-DNA MISMATCH REPAIR AS A CAUSE OF COLON-CANCER

      Pathologie et biologie
    61. XIE YG; HAN FY; BAJALICA S; BLENNOW E; KRISTOFFERSSON U; DUMANSKI JP; NORDENSKJOLD M
      IDENTIFICATION, CHARACTERIZATION AND CLINICAL-APPLICATIONS OF COSMIDSFROM THE TELOMERIC AND CENTROMERIC REGIONS OF THE LONG ARM OF CHROMOSOME-22

      Human genetics
    62. ZELADAHEDMAN M; TORROELLA M; MESQUITA R; NORDENSKJOLD M; SKOOG L; LINDBLOM A
      LOSS OF HETEROZYGOSITY STUDIES IN TUMORS FROM FAMILIES WITH BREAST-OVARIAN CANCER SYNDROME

      Human genetics
    63. TANNERGARD P; ZABAROVSKY E; STANBRIDGE E; NORDENSKJOLD M; LINDBLOM A
      SUBLOCALIZATION OF A LOCUS AT 3P21.3-23 PREDISPOSING TO HEREDITARY NONPOLYPOSIS COLON-CANCER

      Human genetics
    64. ZELADAHEDMAN M; WERER G; COLLINS P; BACKDAHL M; PEREZ I; FRANCO S; JIMENEZ J; CRUZ J; TORROELLA M; NORDENSKJOLD M; SKOOG L; LINDBLOM A
      HIGH EXPRESSION OF THE EGFR IN FIBROADENOMAS COMPARED TO BREAST CARCINOMAS

      Anticancer research
    65. BLENNOW E; BUI TH; KRISTOFFERSSON U; VUJIC M; ANNEREN G; HOLMBERG E; NORDENSKJOLD M
      SWEDISH SURVEY ON EXTRA STRUCTURALLY ABNORMAL CHROMOSOMES IN 39105 CONSECUTIVE PRENATAL DIAGNOSES - PREVALENCE AND CHARACTERIZATION BY FLUORESCENCE IN-SITU HYBRIDIZATION

      Prenatal diagnosis
    66. KOLODNER RD; HALL NR; LIPFORD J; KANE MF; RAO MRS; MORRISON P; WIRTH L; FINAN PJ; BURN J; CHAPMAN P; EARABINO C; MERCHANT E; BISHOP DT; GARBER J; BRONNER CE; BAKER SM; WARREN G; SMITH LG; LINDBLOM A; TANNERGARD P; BOLLAG RJ; GODWIN AR; WARD DC; NORDENSKJOLD M; LISKAY RM; COPELAND N; JENKINS N; LESCOE MK; EWEL A; LEE S; GRIFFITH J; FISHEL R
      HUMAN MISMATCH REPAIR GENES AND THEIR ASSOCIATION WITH HEREDITARY NONPOLYPOSIS COLON-CANCER

      Cold Spring Harbor Symposia on Quantitative Biology
    67. BRONNER CE; BAKER SM; MORRISON PT; WARREN G; SMITH LG; LESCOE MK; KANE M; EARABINO C; LIPFORD J; LINDBLOM A; TANNERGARD P; BOLLAG RJ; GODWIN AR; WARD DC; NORDENSKJOLD M; FISHEL R; KOLODNER R; LISKAY RM
      MUTATION IN THE DNA MISMATCH REPAIR GENE HOMOLOG HMLH1 IS ASSOCIATED WITH HEREDITARY NONPOLYPOSIS COLON-CANCER

      Nature
    68. FRIEDMAN E; BALE AE; CARSON E; BOSON WL; NORDENSKJOLD M; RITZEN M; FERREIRA PC; JAMMAL A; DEMARCO L
      NEPHROGENIC DIABETES-INSIPIDUS - AN X-CHROMOSOME-LINKED DOMINANT INHERITANCE PATTERN WITH A VASOPRESSIN TYPE-2 RECEPTOR GENE THAT IS STRUCTURALLY NORMAL

      Proceedings of the National Academy of Sciences of the United Statesof America
    69. TEH BT; HAYWARD NK; WALTERS MK; SHEPHERD JJ; WILKINSON S; NORDENSKJOLD M; LARSSON C
      GENETIC-STUDIES OF THYMIC CARCINOIDS IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-1

      Journal of Medical Genetics
    70. FRIEDMAN E; ADAMS EF; HOOG A; GEJMAN PV; CARSON E; LARSSON C; DEMARCO L; WERNER S; FAHLBUSCH R; NORDENSKJOLD M
      NORMAL STRUCTURAL DOPAMINE TYPE-2 RECEPTOR GENE IN PROLACTIN-SECRETING AND OTHER PITUITARY-TUMORS

      The Journal of clinical endocrinology and metabolism
    71. JANSON M; NORDENSKJOLD M
      A CONSTITUTIONAL MUTATION WITHIN THE RETINOBLASTOMA GENE DETECTED BY PFGE

      Clinical genetics
    72. LINDBLOM A; SANDELIN K; ISELIUS L; DUMANSKI J; WHITE I; NORDENSKJOLD M; LARSSON C
      PREDISPOSITION FOR BREAST-CANCER IN CARRIERS OF CONSTITUTIONAL TRANSLOCATION 11Q22Q

      American journal of human genetics
    73. BLENNOW E; TELENIUS H; DEVOS D; LARSSON S; HENRIKSSON P; JOHANSSON O; CARTER NP; NORDENSKJOLD M
      TETRASOMY 15Q - 2 MARKER CHROMOSOMES WITH NO DETECTABLE ALPHA-SATELLITE DNA

      American journal of human genetics
    74. LINDBLOM A; TANNERGARD P; WERELIUS B; NORDENSKJOLD M
      GENETIC-MAPPING OF A 2ND LOCUS PREDISPOSING TO HEREDITARY NONPOLYPOSIS COLON-CANCER

      Nature genetics
    75. XIE YG; HAN FY; PEYRARD M; RUTTLEDGE MH; FRANSSON I; DEJONG P; COLLINS J; DUNHAM I; NORDENSKJOLD M; DUMANSKI JP
      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
    76. KAS K; SCHOENMAKERS E; VANDEVEN W; WEBER G; NORDENSKJOLD M; MICHIELS L; MERREGAERT J; LARSSON C
      ASSIGNMENT OF THE HUMAN FAU GENE TO A SUBREGION OF CHROMOSOME-11Q13

      Genomics
    77. NORDENSKJOLD A; HEDBORG F; LUTHMAN H; NORDENSKJOLD M
      TIGHT LINKAGE BETWEEN THE BECKWITH-WIEDEMANN SYNDROME AND A MICROSATELLITE MARKER FOR THE TH LOCUS

      Human genetics
    78. KARLBOM AE; JAMES CD; BOETHIUS J; CAVENEE WK; COLLINS VP; NORDENSKJOLD M; LARSSON C
      LOSS OF HETEROZYGOSITY IN MALIGNANT GLIOMAS INVOLVES AT LEAST 3 DISTINCT REGIONS ON CHROMOSOME-10

      Human genetics
    79. RUTTLEDGE MH; NAROD SA; DUMANSKI JP; PARRY DM; ELDRIDGE R; WERTELECKI W; PARBOOSINGH J; FAUCHER MC; LENOIR GM; COLLINS VP; NORDENSKJOLD M; ROULEAU GA
      PRESYMPTOMATIC DIAGNOSIS FOR NEUROFIBROMATOSIS-2 WITH CHROMOSOME-22 MARKERS

      Neurology
    80. WASSIF WS; MONIZ CF; FRIEDMAN E; WONG S; WEBER G; NORDENSKJOLD M; PETERS TJ; LARSSON C
      FAMILIAL ISOLATED HYPERPARATHYROIDISM - A DISTINCT GENETIC ENTITY WITH AN INCREASED RISK OF PARATHYROID CANCER

      The Journal of clinical endocrinology and metabolism
    81. TORDJMAN K; STERN N; OUAKNINE G; YOSSIPHOV Y; RAZON N; NORDENSKJOLD M; FRIEDMAN E
      ACTIVATING MUTATIONS OF THE GS ALPHA-GENE IN NONFUNCTIONING PITUITARY-TUMORS

      The Journal of clinical endocrinology and metabolism
    82. LINDBLOM A; SKOOG L; ROTSTEIN S; WERELIUS B; LARSSON C; NORDENSKJOLD M
      LOSS OF HETEROZYGOSITY IN FAMILIAL BREAST CARCINOMAS

      Cancer research
    83. LINDBLOM A; ROTSTEIN S; SKOOG L; NORDENSKJOLD M; LARSSON C
      DELETIONS ON CHROMOSOME-16 IN PRIMARY FAMILIAL BREAST CARCINOMAS ARE ASSOCIATED WITH DEVELOPMENT OF DISTANT METASTASES

      Cancer research
    84. FRIEDMAN E; ADAMS EF; HOOG A; GEJMAN PV; CARSON E; LARSSON C; DEMARCO L; WERNER S; FAHLBUSCH R; NORDENSKJOLD M
      NORMAL STRUCTURAL DOPAMINE TYPE-2 RECEPTOR GENE IN PROLACTIN-SECRETING AND OTHER PITUITARY-TUMORS

      American journal of human genetics
    85. DEMARCO L; BALE AE; CARSON E; BOSON W; NORDENSKJOLD M; RITZEN M; FERREIRA PC; FRIEDMAN E
      NEPHROGENIC DIABETES-INSIPIDUS - A NOVEL X-LINKED DOMINANT INHERITANCE PATTERN AND NORMAL STRUCTURAL V2 RECEPTOR GENE

      American journal of human genetics
    86. XIE YG; HAN FY; RUTTLEDGE MH; FRANSSON I; PEYRARD M; DUNHAM I; COLLINS J; DEJONG P; NORDENSKJOLD M; DUMANSKI JP
      CONSTRUCTION OF YAC AND COSMID CONTIG IN THE NEUROFIBROMATOSIS TYPE-2(NF2) AND MENINGIOMA REGION ON CHROMOSOME-22Q12

      American journal of human genetics
    87. HAN FY; XIE YG; BAJALICA S; BLENNOW E; NORDENSKJOLD M; DUMANSKI JP
      ESTABLISHING OF COSMID CONTIGS IN THE SUBCENTROMERIC AND SUBTELOMERICREGIONS OF THE LONG ARM OF HUMAN CHROMOSOME-22

      American journal of human genetics
    88. BLENNOW E; ANNEREN G; BUI TH; BERGGREN E; ASADI E; NORDENSKJOLD M
      CHARACTERIZATION OF SUPERNUMERARY RING MARKER CHROMOSOMES BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH)

      American journal of human genetics
    89. LINDBLOM A; ROTSTEIN S; NORDENSKJOLD M; LARSSON C
      LINKAGE ANALYSIS WITH MARKERS ON 17Q IN 29 SWEDISH BREAST-CANCER FAMILIES

      American journal of human genetics
    90. LARSSON C; WEBER G; NORDENSKJOLD M; FRIEDMAN E; SKOGSEID B; OBERG K; SHEPHERD J; TEH B; HAYWARD N; GRIMMOND S
      GENETIC-ASPECTS OF TUMOR-DEVELOPMENT IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-1

      Diagnostic oncology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 30/10/20 alle ore 15:07:38