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    1. Vorechovsky, I; Kralovicova, J; Tchilian, E; Masterman, T; Zhang, ZP; Ferry, B; Misbah, S; Chapel, H; Webster, D; Hellgren, D; Anvret, M; Hillert, J; Hammarstrom, L; Beverley, PC
      Does 77C -> G in PTPRC modify autoimmune disorders linked to the major histocompatibility locus?

      NATURE GENETICS
    2. Kerr, AM; Nomura, Y; Armstrong, D; Anvret, M; Belichenko, PV; Budden, S; Cass, H; Christodoulou, J; Clarke, A; Ellaway, C; d'Esposito, M; Francke, U; Hulten, M; Julu, P; Leonard, H; Naidu, S; Schanen, C; Webb, T; Engerstrom, IW; Yamashita, Y; Segawa, M
      Guidelines for reporting clinical features in cases with MECP2 mutations

      BRAIN & DEVELOPMENT
    3. Xiang, F; Stenbom, Y; Anvret, M; Hagberg, B
      Closely related Swedish Rett syndrome females - None with MECP2 mutation revealed

      NEUROPEDIATRICS
    4. Villard, L; Levy, N; Xiang, FQ; Kpebe, A; Labelle, V; Chevillard, C; Zhang, ZP; Schwartz, CE; Tardieu, M; Chelly, J; Anvret, M; Fontes, M
      Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications forthe disease

      JOURNAL OF MEDICAL GENETICS
    5. Eriksson, M; Ansved, T; Anvret, M; Carey, N
      A mammalian Radial Spokehead-Like gene, RSHL1, at the myotonic dystrophy-llocus

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    6. Moore, RC; Xiang, FQ; Monaghan, J; Han, D; Zhang, ZP; Edstrom, L; Anvret, M; Prusiner, SB
      Huntington disease phenocopy is a familial prion disease

      AMERICAN JOURNAL OF HUMAN GENETICS
    7. Buervenich, S; Sydow, O; Carmine, A; Zhang, ZP; Anvret, M; Olson, L
      Alcohol dehydrogenase alleles in Parkinson's disease

      MOVEMENT DISORDERS
    8. Buervenich, S; Carmine, A; Arvidsson, M; Xiang, FQ; Zhang, ZP; Sydow, O; Jonsson, EG; Sedvall, GC; Leonard, S; Ross, RG; Freedman, R; Chowdari, KV; Nimgaonkar, VL; Perlmann, T; Anvret, M; Olson, L
      NURR1 mutations in cases of schizophrenia and manic-depressive disorder

      AMERICAN JOURNAL OF MEDICAL GENETICS
    9. Xiang, FQ; Buervenich, S; Nicolao, P; Bailey, MES; Zhang, ZP; Anvret, M
      Mutation screening in Rett syndrome patients

      JOURNAL OF MEDICAL GENETICS
    10. Eriksson, M; Ansved, T; Edstrom, L; Wells, DJ; Watt, DJ; Anvret, M; Carey, N
      Independent regulation of the myotonic dystrophy 1 locus genes postnatallyand during adult skeletal muscle regenerator

      JOURNAL OF BIOLOGICAL CHEMISTRY
    11. Wahlin, TBR; Backman, L; Lundin, A; Haegermark, A; Winblad, B; Anvret, M
      High suicidal ideation in persons testing for Huntington's disease

      ACTA NEUROLOGICA SCANDINAVICA
    12. Hedberg, B; Anvret, M; Ansved, T
      CTG-repeat length in distal and proximal leg muscles of symptomatic and non-symptomatic patients with myotonic dystrophy: relation to muscle strengthand degree of histopathological abnormalities

      EUROPEAN JOURNAL OF NEUROLOGY
    13. Eriksson, N; Ansved, T; Edstrom, L; Anvret, M; Carey, N
      Simultaneous analysis of expression of the three myotonic dystrophy locus genes in adult skeletal muscle samples: the CTG expansion correlates inversely with DMPK and 59 expression levels, but not DMAHP levels

      HUMAN MOLECULAR GENETICS
    14. Xiang, FQ; Nicolao, P; Chapon, F; Edstrom, L; Anvret, M; Zhang, ZP
      A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21

      NEUROMUSCULAR DISORDERS
    15. Ahlberg, G; von Tell, D; Borg, K; Edstrom, L; Anvret, M
      Genetic linkage of Welander distal myopathy to chromosome 2p13

      ANNALS OF NEUROLOGY
    16. Nordenskjold, A; Friedman, E; Tapper-Persson, M; Soderhall, C; Leviav, A; Svensson, J; Anvret, M
      Screening for mutations in candidate genes for hypospadias

      UROLOGICAL RESEARCH
    17. Svensson, PJ; Von Tell, D; Molander, ML; Anvret, M; Nordenskjold, A
      A heterozygous frameshift mutation in the endothelin-3 (EDN-3) gene in isolated Hirschsprung's disease

      PEDIATRIC RESEARCH
    18. Tscherning-Casper, C; Papadogiannakis, N; Anvret, M; Stolpe, L; Lindgren, S; Bohlin, AB; Albert, J; Fenyo, EM
      The trophoblastic epithelial barrier is not infected in full-term placentae of human immunodeficiency virus-seropositive mothers undergoing antiretroviral therapy

      JOURNAL OF VIROLOGY
    19. Svensson, PJ; Tapper-Persson, M; Anvret, M; Molander, ML; Eng, C; Nordenskjold, A
      Mutations in the endothelin-receptor B gene in Hirschsprung disease in Sweden

      CLINICAL GENETICS
    20. Nicolao, P; Xiang, FQ; Gunnarsson, LG; Giometto, B; Edstrom, L; Anvret, M; Zhang, ZP
      Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2q

      AMERICAN JOURNAL OF HUMAN GENETICS
    21. Zhang, ZP; Eriksson, M; Falk, G; Graff, C; Presnell, SC; Read, MS; Nichols, TC; Blomback, M; Anvret, M
      Failure to achieve gene conversion with chimeric circular oligonucleotides: Potentially misleading PCR artifacts observed

      ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT
    22. GRIGELIONIENE G; HAGENAS L; EKLOF O; NEUMEYER L; HAEREID PE; ANVRET M
      A NOVEL MISSENSE MUTATION-ILE538VAL IN THE FIBROBLAST-GROWTH-FACTOR-RECEPTOR-3 IN HYPOCHONDROPLASIA

      Human mutation
    23. AHLBERG G; BORG K; EDSTROM L; ANVRET M
      WELANDER HEREDITARY DISTAL MYOPATHY, A MOLECULAR-GENETIC COMPARISON TO HEREDITARY MYOPATHIES WITH INCLUSION-BODIES

      Neuromuscular disorders
    24. BORG K; AHLBERG G; ANVRET M; EDSTROM L
      WELANDER-DISTAL-MYOPATHY - AN OVERVIEW

      Neuromuscular disorders
    25. SVENSSON PJ; ANVRET M; MOLANDER ML; NORDENSKJOLD A
      PHENOTYPIC VARIATION IN A FAMILY WITH MUTATIONS IN 2 HIRSCHSPRUNG-RELATED GENES (RET AND ENDOTHELIN RECEPTOR-B)

      Human genetics
    26. ANSVED T; LUNDIN A; ANVRET M
      LARGER CAG EXPANSIONS IN SKELETAL-MUSCLE COMPARED WITH LYMPHOCYTES INKENNEDY-DISEASE BUT NOT IN HUNTINGTON-DISEASE

      Neurology
    27. XIANG FQ; ZHANG ZP; CLARKE A; JOSELUIZ P; SAKKUBAI N; SAROJINI B; DELOZIERBLANCHET CD; HANSMANN I; EDSTROM L; ANVRET M
      CHROMOSOME MAPPING OF RETT-SYNDROME - A LIKELY CANDIDATE REGION ON THE TELOMERE OF XQ

      Journal of Medical Genetics
    28. SVENSSON PJ; MOLANDER ML; ENG C; ANVRET M; NORDENSKJOLD A
      LOW-FREQUENCY OF RET MUTATIONS IN HIRSCHSPRUNG DISEASE IN SWEDEN

      Clinical genetics
    29. XIANG FQ; ALMQVIST EW; HUQ M; LUNDIN A; HAYDEN MR; EDSTROM L; ANVRET M; ZHANG Z
      A HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER MAPS TO CHROMOSOME 20P

      American journal of human genetics
    30. ANVRET M; CLARKE A
      GENETICS AND RETT-SYNDROME

      European child & adolescent psychiatry
    31. THOMAS NST; DAVIES K; WEBB T; WILLIAMS N; PRICE W; OWEN M; PEREIRA J; KERR A; ANVRET M; HANEFELD E; CLARKE A
      MOLECULAR-GENETIC STUDIES IN FAMILIAL RETT-SYNDROME

      European child & adolescent psychiatry
    32. ZHANG Z; XIANG F; ANVRET M
      GENE-MAPPING OF THE RETT-SYNDROME

      European child & adolescent psychiatry
    33. KROISEL PM; FRYNS JP; MATTHIJS G; BRONDUMNIELSEN K; VEJERSLEV L; VONKOSKULL H; GIRAUDON E; SAURA R; HELD K; MULLERREIBLE CR; METAXOTOU C; GENUARDI M; PIOMBO G; SCHNEIDER F; SMEETS D; VANDENOUWELAND A; PACHECO P; CORREIA H; BINKERT F; GABARRON J; GALLANO P; KRISTOFFERSSON U; ANVRET M; HOWELL R; STENHOUSE S
      QUALITY GUIDELINES AND STANDARDS FOR GENETIC LABORATORIES CLINICS IN PRENATAL-DIAGNOSIS ON FETAL SAMPLES OBTAINED BY INVASIVE PROCEDURES - AN ATTEMPT TO ESTABLISH A COMMON EUROPEAN FRAMEWORK FOR QUALITY ASSESSMENT/

      European journal of human genetics
    34. BORG K; AHLBERG G; ANVRET M
      C4342T-MUTATION IN THE SCN4A GENE ON CHROMOSOME 17Q IN A SWEDISH FAMILY WITH PARAMYOTONIA-CONGENITA (EULENBURG) - CORRELATIONS WITH CLINICAL, NEUROPHYSIOLOGICAL AND MUSCLE BIOPSY DATA

      Neuromuscular disorders
    35. AHLBERG G; BORG K; EDSTROM L; ANVRET M
      WELANDER DISTAL MYOPATHY IS NOT LINKED TO OTHER DEFINED DISTAL MYOPATHY GENE LOCI

      Neuromuscular disorders
    36. ANSVED T; EDSTROM L; GRANDELL U; HEDBERG B; ANVRET M
      VARIATION OF CTG-REPEAT NUMBER OF THE DMPK GENE IN MUSCLE-TISSUE

      Neuromuscular disorders
    37. ZHANG ZP; ERIKSSON M; BLOMBACK M; ANVRET M
      A NEW APPROACH TO GENE-THERAPY

      Blood coagulation & fibrinolysis
    38. ZHANG ZP; BLOMBACK M; ANVRET M
      UNDERSTANDING VON-WILLEBRANDS-DISEASE FROM GENE DEFECTS TO THE PATIENTS

      Journal of internal medicine
    39. MALM G; RINGDEN O; ANVRET M; VONDOBELN U; HAGENFELDT L; ISBERG B; KNUUTILA S; NENNESMO I; WINIARSKI J; MARCUS C
      TREATMENT OF ADRENOLEUKODYSTROPHY WITH BONE-MARROW TRANSPLANTATION

      Acta paediatrica
    40. CASTORA F; HART C; BURGESS C; ANVRET M; NAIDU SB; LEWIS D
      IS THERE A GENETIC-MARKER FOR RETT-SYNDROME ON MITOCHONDRIAL-DNA - ANALYSIS OF THE 22 TRANSFER-RNA GENES

      Annals of neurology
    41. LUNDIN G; LEE JS; THUNELL S; ANVRET M
      GENETIC INVESTIGATION OF THE PORPHOBILINOGEN DEAMINASE GENE IN SWEDISH ACUTE INTERMITTENT PORPHYRIA FAMILIES

      Human genetics
    42. WAHLIN TBR; LUNDIN A; BACKMAN L; ALMQVIST E; HAEGERMARK A; WINBLAD B; ANVRET M
      REACTIONS TO PREDICTIVE TESTING IN HUNTINGTON DISEASE - CASE-REPORTS OF COPING WITH A NEW GENETIC STATUS

      American journal of medical genetics
    43. LINDGREN AC; MARCUS C; SKWIRUT C; ELIMAM A; HAGENAS L; SCHALLING M; ANVRET M; LONNQVIST F
      INCREASED LEPTIN MESSENGER-RNA AND SERUM LEPTIN LEVELS IN CHILDREN WITH PRADER-WILLI-SYNDROME AND NONSYNDROMAL OBESITY

      Pediatric research
    44. LUNDIN G; ANVRET M
      CHARACTERIZATION AND REGULATION OF THE NONERYTHROID PORPHOBILINOGEN DEAMINASE PROMOTER

      Biochemical and biophysical research communications
    45. ALMQVIST E; CHONG SS; NICHOL K; TELENIUS H; LATRAY L; BOURDELATPARKS B; HADDAD BR; SQUITIERI F; ANVRET M; VANDENENGH G; HAYDEN M
      DIFFERENT MUTATION-RATES OF SIMILAR SIZED CAG TRACTS OF AFFECTED HUNTINGTON-DISEASE CHROMOSOMES BY SINGLE SPERM ANALYSIS

      American journal of human genetics
    46. CASTORA F; BURGESS C; HART C; LEWIS D; NAIDU S; ANVRET M; ZHANG Z; XIANG F
      MITOCHONDRIAL-DNA AND RETT-SYNDROME - A SEARCH FOR A GENETIC-MARKER

      American journal of human genetics
    47. LINDGREN AC; GRANDELL U; RITZEN EM; ANVRET M
      DIAGNOSIS OF THE PRADER-WILLI-SYNDROME BY PROVING THE ABSENCE OF THE UNMETHYLATED PW71 DNA FRAGMENT

      Acta paediatrica
    48. ALDERBORN A; ANVRET M; GUSTAVSON KH; HAGENAS L; WADELIUS C
      ACHONDROPLASIA IN SWEDEN CAUSED BY THE G1138A MUTATION IN FGFR3

      Acta paediatrica
    49. WESTGREN M; RINGDEN O; EIKNES S; EK S; ANVRET M; BRUBAKK AM; BUI TH; GIAMBONA A; KISERUD T; KJAELDGAARD A; MAGGIO A; MARKLING L; SEIGER A; ORLANDI F
      LACK OF EVIDENCE OF PERMANENT ENGRAFTMENT AFTER IN-UTERO FETAL STEM-CELL TRANSPLANTATION IN CONGENITAL HEMOGLOBINOPATHIES

      Transplantation
    50. NORDENSKJOLD A; TAPPERPERSSON M; ANVRET M
      NO EVIDENCE OF WT1 GENE-MUTATIONS IN CHILDREN WITH CONGENITAL DIAPHRAGMATIC-HERNIA

      Journal of pediatric surgery
    51. CAREY N; JOHNSON K; NOKELAINEN P; PELTONEN L; SAVONTAUS ML; JUVONEN V; ANVRET M; GRANDELL U; CHOTAI K; ROBERTSON E; MIDDLETONPRICE H; MALCOLM S
      MEIOTIC DRIVE AND MYOTONIC-DYSTROPHY - REPLY

      Nature genetics
    52. TELENIUS H; ALMQVIST E; KREMER B; SPENCE N; SQUITIERI F; NICHOL K; GRANDELL U; STARR E; BENJAMIN C; CASTALDO I; CALABRESE O; ANVRET M; GOLDBERG YP; HAYDEN MR
      SOMATIC MOSAICISM IN SPERM IS ASSOCIATED WITH INTERGENERATIONAL (CAG)N CHANGES IN HUNTINGTON DISEASE (VOL 4, PG 189, 1995)

      Human molecular genetics
    53. TELENIUS H; ALMQVIST E; KREMER B; SPENCE N; SQUITIERI F; NICHOL K; GRANDELL U; STARR E; BENJAMIN C; CASTALDO I; CALABRESE O; ANVRET M; GOLDBERG YP; HAYDEN MR
      SOMATIC MOSAICISM IN SPERM IS ASSOCIATED WITH INTERGENERATIONAL (CAG)(N) CHANGES IN HUNTINGTON DISEASE

      Human molecular genetics
    54. ALMQVIST E; SPENCE N; NICHOL K; ANDREW SE; VESA J; PELTONEN L; ANVRET M; GOTO J; KANAZAWA I; GOLDBERG YP; HAYDEN MR
      ANCESTRAL DIFFERENCES IN THE DISTRIBUTION OF THE DELTA-2642 GLUTAMIC-ACID POLYMORPHISM IS ASSOCIATED WITH VARYING CAG REPEAT LENGTHS ON NORMAL CHROMOSOMES - INSIGHTS INTO THE GENETIC EVOLUTION OF HUNTINGTON DISEASE

      Human molecular genetics
    55. ANDERSSON C; THUNELL S; FLODERUS Y; FORSELL C; LUNDIN G; ANVRET M; LANNFELT L; WETTERBERG L; LITHNER F
      DIAGNOSIS OF ACUTE INTERMITTENT PORPHYRIA IN NORTHERN SWEDEN - AN EVALUATION OF MUTATION ANALYSIS AND BIOCHEMICAL METHODS

      Journal of internal medicine
    56. TELENIUS H; ALMQVIST E; KREMER B; SPENCE N; NICHOL K; SQUITIERI F; THEILMANN J; ANVRET M; GOLDBERG YP; HAYDEN MR
      MECHANISMS UNDERLYING (CAG) EXPANDION IN HUNTINGTON DISEASE INCLUDE TISSUE-SPECIFIC AND CIS-ACTING FACTORS

      Journal of cellular biochemistry
    57. ZHANG ZP; LINDSTEDT M; BLOMBACK M; ANVRET M
      EFFECTS OF THE MUTANT VON-WILLEBRAND-FACTOR GENE IN VON-WILLEBRAND DISEASE

      Human genetics
    58. NORDENSKJOLD A; FRICKE G; ANVRET M
      ABSENCE OF MUTATIONS IN THE WT1 GENE IN PATIENTS WITH XY GONADAL-DYSGENESIS

      Human genetics
    59. ZHANG ZP; BLOMBACK M; ANVRET M
      EFFECTS OF THE MUTANT VON-WILLEBRAND-FACTOR GENE IN VON-WILLEBRAND DISEASE

      Thrombosis and haemostasis
    60. ANVRET M; ZHANG ZP
      CURRENT STATUS OF GENETIC RESEARCH IN RETT-SYNDROME

      Neuropediatrics
    61. LUNDIN G; HASHEMI J; FLODERUS Y; THUNELL S; SAGEN E; LAEGREID A; WASSIF W; PETERS T; ANVRET M
      4 MUTATIONS IN THE PORPHOBILINOGEN DEAMINASE GENE IN PATIENTS WITH ACUTE INTERMITTENT PORPHYRIA

      Journal of Medical Genetics
    62. NORDENSKJOLD A; FRIEDMAN E; SANDSTEDT B; SODERHALL S; ANVRET M
      CONSTITUTIONAL AND SOMATIC MUTATIONS IN THE WT1 GENE IN WILMS-TUMOR PATIENTS

      International journal of cancer
    63. AKEFELDT A; ANVRET M; GRANDELL U; NORDLINDER R; GILLBERG C
      PARENTAL EXPOSURE TO HYDROCARBONS IN PRADER-WILLI-SYNDROME

      Developmental Medicine and Child Neurology
    64. MORRAL N; BERTRANPETIT J; ESTIVILL X; NUNES V; CASALS T; GIMENEZ J; REIS A; VARONMATEEVA R; MACEK M; KALAYDJIEVA L; ANGELICHEVA D; DANCHEVA R; ROMEO G; RUSSO MP; GARNERONE S; RESTAGNO G; FERRARI M; MAGNANI C; CLAUSTRES M; DESGEORGES M; SCHWARTZ M; SCHWARZ M; DALLAPICCOLA B; NOVELLI G; FEREC C; DEARCE M; NEMETI M; KERE T; ANVRET M; DAHL N; KADASI L
      THE ORIGIN OF THE MAJOR CYSTIC-FIBROSIS MUTATION (DELTA-F508) IN EUROPEAN POPULATIONS

      Nature genetics
    65. CAREY N; JOHNSON K; NOKELAINEN P; PELTONEN L; SAVONTAUS ML; JUVONEN V; ANVRET M; GRANDELL U; CHOTAI K; ROBERTSON E; MIDDLETONPRICE H; MALCOLM S
      MEIOTIC DRIVE AT THE MYOTONIC-DYSTROPHY LOCUS

      Nature genetics
    66. BUI TH; ANVRET M; DAHL N; GAROFF L; SJOBLOM P; HILLENSJO T
      COMPLEX GENETIC-COUNSELING AND EXCLUSION OF DUCHENNE MUSCULAR-DYSTROPHY IN A TWIN PREGNANCY AFTER IN-VITRO FERTILIZATION (IVF)

      Journal of assisted reproduction and genetics
    67. SQUITIERI F; ANDREW SE; GOLDBERG YP; KREMER B; SPENCE N; ZEISLER J; NICHOL K; THEILMANN J; GREENBERG J; GOTO J; KANAZAWA I; VESA J; PELTONEN L; ALMQVIST E; ANVRET M; TELENIUS H; LIN B; NAPOLITANO G; MORGAN K; HAYDEN MR
      DNA HAPLOTYPE ANALYSIS OF HUNTINGTON DISEASE REVEALS CLUES TO THE ORIGINS AND MECHANISMS OF CAG EXPANSION AND REASONS FOR GEOGRAPHIC VARIATIONS OF PREVALENCE

      Human molecular genetics
    68. SEDVALL G; KARLSSON P; LUNDIN A; ANVRET M; SUHARA T; HALLDIN C; FARDE L
      DOPAMINE D-1 RECEPTOR NUMBER - A SENSITIVE PET MARKER FOR EARLY BRAINDEGENERATION IN HUNTINGTONS-DISEASE

      European archives of psychiatry and clinical neuroscience
    69. ZHANG ZP; BLOMBACK M; EGBERG N; FALK G; ANVRET M
      CHARACTERIZATION OF THE VON-WILLEBRAND-FACTOR GENE (VWF) IN VON-WILLEBRAND DISEASE TYPE-III PATIENTS FROM 24 FAMILIES OF SWEDISH AND FINNISH ORIGIN

      Genomics
    70. ALMQVIST E; ANDREW S; THEILMANN J; GOLDBERG P; ZEISLER J; DRUGGE U; GRANDELL U; TAPPERPERSSON M; WINBLAD B; HAYDEN M; ANVRET M
      GEOGRAPHICAL-DISTRIBUTION OF HAPLOTYPES IN SWEDISH FAMILIES WITH HUNTINGTONS-DISEASE

      Human genetics
    71. NORDENSKJOLD A; FRIEDMAN E; ANVRET M
      WT1 MUTATIONS IN PATIENTS WITH DENYS-DRASH SYNDROME - A NOVEL MUTATION IN EXON-8 AND PATERNAL ALLELE ORIGIN

      Human genetics
    72. SCHWARTZ M; ANVRET M; CLAUSTRES M; EIKEN HG; EIKLID K; SCHAEDEL C; STOLPE L; TRANEBJAERG L
      394DELTT - A NORDIC CYSTIC-FIBROSIS MUTATION

      Human genetics
    73. LUNDIN G; WEDELL A; THUNELL S; ANVRET M
      2 NEW MUTATIONS IN THE PORPHOBILINOGEN DEAMINASE GENE AND A SCREENINGMETHOD USING PCR AMPLIFICATION OF SPECIFIC ALLELES

      Human genetics
    74. ANVRET M; WAHLSTROM J
      RETT-SYNDROME - RANDOM X-CHROMOSOME INACTIVATION

      Clinical genetics
    75. REIS A; DITTRICH B; GREGER V; BUITING K; LALANDE M; GILLESSENKAESBACH G; ANVRET M; HORSTHEMKE B
      IMPRINTING MUTATIONS SUGGESTED BY ABNORMAL DNA METHYLATION PATTERNS IN FAMILIAL ANGELMAN AND PRADER-WILLI SYNDROMES

      American journal of human genetics
    76. ANDREW SE; GOLDBERG YP; KREMER B; SQUITIERI F; THEILMANN J; ZEISLER J; TELENIUS H; ADAM S; ALMQUIST E; ANVRET M; LUCOTTE G; STOESS AJ; CAMPANELLA G; HAYDEN MR
      HUNTINGTON DISEASE WITHOUT CAG EXPANSION - PHENOCOPIES OR ERRORS IN ASSIGNMENT

      American journal of human genetics
    77. ASHIZAWA T; ANVRET M; BAIGET M; BARCELO JM; BRUNNER H; COBO AM; DALLAPICCOLA B; FENWICK RG; GRANDELL U; HARLEY H; JUNIEN C; KOCH MC; KORNELUK RG; LAVEDAN C; MIKI T; MULLEY JC; DEMUNAIN AL; NOVELLI G; ROSES AD; SELTZER WK; SHAW DJ; SMEETS H; SUTHERLAND GR; YAMAGATA H; HARPER PS
      CHARACTERISTICS OF INTERGENERATIONAL CONTRACTIONS OF THE CTG REPEAT IN MYOTONIC-DYSTROPHY

      American journal of human genetics
    78. ANVRET M; AHLBERG G; GRANDELL U; HEDBERG B; JOHNSON K; EDSTROM L
      LARGER EXPANSIONS OF THE CTG REPEAT IN MUSCLE COMPARED TO LYMPHOCYTESFROM PATIENTS WITH MYOTONIC-DYSTROPHY

      Human molecular genetics
    79. TELENIUS H; KREMER HPH; THEILMANN J; ANDREW SE; ALMQVIST E; ANVRET M; GREENBERG C; GREENBERG J; LUCOTTE G; SQUITIERI F; STARR E; GOLDBERG YP; HAYDEN MR
      MOLECULAR ANALYSIS OF JUVENILE HUNTINGTON DISEASE - THE MAJOR INFLUENCE ON (CAG)(N) REPEAT LENGTH IS THE SEX OF THE AFFECTED PARENT

      Human molecular genetics
    80. DAHL N; GRANDELL U; MARTINSSON T; ALLEN M; JOHANSSON L; STOLPE L; GYLLENSTEN U; HJELTE L; KOLLBERG H; STRANDVIK B; WAHLSTROM J; ANVRET M
      FREQUENCY OF 4 CYSTIC-FIBROSIS MUTATIONS IN A SWEDISH POPULATION

      Acta paediatrica
    81. BLOMBACK M; ZHANG ZP; NYMAN D; ANVRET M
      MUTATIONS OF THE VON-WILLEBRAND-FACTOR GENE IN THE PATIENTS WITH VON-WILLEBRANDS DISEASE IN THE ALAND ISLAND

      Thrombosis and haemostasis
    82. ZHANG ZP; FALK G; EGBERG N; BLOMBACK M; ANVRET M
      MUTATION SCREENING OF THE VON-WILLEBRAND-FACTOR GENE IN VON-WILLEBRAND DISEASE TYPE-I AND TYPE-III PATIENTS

      Thrombosis and haemostasis
    83. SAGEN E; LAEGREID A; ANVRET M; LUNDIN G; LANNFELT L; LILIUS L; FLODERUS Y; ROMSLO I
      GENETIC CARRIER DETECTION IN NORWEGIAN FAMILIES WITH ACUTE INTERMITTENT PORPHYRIA

      Scandinavian journal of clinical & laboratory investigation
    84. ZHANG ZP; BLOMBACK M; NYMAN D; ANVRET M
      MUTATIONS OF VON-WILLEBRAND-FACTOR GENE IN FAMILIES WITH VON-WILLEBRAND DISEASE IN THE ALAND-ISLANDS

      Proceedings of the National Academy of Sciences of the United Statesof America
    85. ANDREW S; THEILMANN J; ALMQVIST E; NORREMOLLE A; LUCOTTE G; ANVRET M; SORENSEN SA; TURPIN JC; HAYDEN MR
      DNA ANALYSIS OF DISTINCT POPULATIONS SUGGESTS MULTIPLE ORIGINS FOR THE MUTATION CAUSING HUNTINGTON DISEASE

      Clinical genetics
    86. ASHIZAWA T; ANVRET M; BAIGET M; BRUNNER H; COBO A; DALLAPICOOLA B; FENWICK RG; HARLEY H; JUNIEN C; KOCH M; KORNELUK RG; LEVEDAN C; MIKI T; NOVELLI G; ROSES AD; SELTZER WK; SMEETS H; HARPER PS
      CHARACTERISTICS OF CONTRACTIONS OF THE CTG REPEAT IN MYOTONIC-DYSTROPHY (DM) OFFSPRING

      American journal of human genetics
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 10/08/20 alle ore 03:32:29