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La ricerca find articoli where authors phrase all words ' Hulten, M' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 32 riferimenti
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    1. Vacca, M; Filippini, F; Budillon, A; Rossi, V; Mercadante, G; Manzati, E; Gualandi, F; Bigoni, S; Trabanelli, C; Pini, G; Calzolari, E; Ferlini, A; Meloni, I; Hayek, G; Zappella, M; Renieri, A; D'Urso, M; D'Esposito, M; MacDonald, F; Kerr, A; Dhanjal, S; Hulten, M
      Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females

      JOURNAL OF MOLECULAR MEDICINE-JMM
    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. Hulten, M
      Non-invasive prenatal diagnosis of Down's syndrome

      LANCET
    4. Scherthan, H; Jerratsch, M; Li, BB; Smith, S; Hulten, M; Lock, T; de Lange, T
      Mammalian meiotic telomeres: Protein composition and redistribution in relation to nuclear pores

      MOLECULAR BIOLOGY OF THE CELL
    5. Cheadle, JP; Gill, H; Fleming, N; Maynard, J; Kerr, A; Leonard, H; Krawczak, M; Cooper, DN; Lynch, S; Thomas, N; Hughes, H; Hulten, M; Ravine, D; Sampson, JR; Clarke, A
      Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location

      HUMAN MOLECULAR GENETICS
    6. Cheadle, JP; Gill, H; Fleming, N; Maynard, J; Kerr, A; Leonard, H; Krawczak, M; Cooper, DN; Lynch, S; Thomas, N; Hughes, H; Hulten, M; Ravine, D; Sampson, JR; Clarke, A
      Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location (vol 9, pg 1119, 2000)

      HUMAN MOLECULAR GENETICS
    7. Hulten, M; Berntsson, T
      The compression/absorption cycle - influence of some major parameters on COP and a comparison with the compression cycle

      INTERNATIONAL JOURNAL OF REFRIGERATION-REVUE INTERNATIONALE DU FROID
    8. Xu, GL; Bestor, TH; Bourc'his, D; Hsieh, CL; Tommerup, N; Bugge, M; Hulten, M; Qu, XY; Russo, JJ; Viegas-Pequignot, E
      Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

      NATURE
    9. VERMA L; MACDONALD F; LEEDHAM P; MCCONACHIE M; DHANJAL S; HULTEN M
      RAPID AND SIMPLE PRENATAL DNA DIAGNOSIS OF DOWNS-SYNDROME

      Lancet
    10. BROWN GM; LEVERSHA M; HULTEN M; FERGUSONSMITH MA; AFFARA NA; FURLONG RA
      GENETIC-ANALYSIS OF MEIOTIC RECOMBINATION IN HUMANS BY USE OF SPERM TYPING - REDUCED RECOMBINATION WITHIN A HETEROZYGOUS PARACENTRIC INVERSION OF CHROMOSOME 9Q32-Q34.3

      American journal of human genetics
    11. WEST SC; BAUMANN P; BENSON FE; STASIAK A; BARLOW A; HULTEN M
      PROTEIN-MEDIATED MOLECULAR-INTERACTIONS IN GENETIC-RECOMBINATION

      The FASEB journal
    12. UCHE U; HULTEN M
      IDENTIFICATION AND CHARACTERIZATION OF 2 SOMATIC-CELL PROTEINS THAT DECONDENSE HUMAN SPERM NUCLEI

      Journal of Medical Genetics
    13. KHAZANEHDARI K; BARLOW A; WATERS J; HULTEN M
      IMMUNOFLUORESCENCE AND MOLECULAR CYTOGENETICS ANALYSIS OF MEIOTIC CHROMOSOME SYNAPSIS, RECOMBINATION AND SEGREGATION IN A HUMAN MALE CARRIER OF A COMPLEX STRUCTURAL CHROMOSOME REARRANGEMENT

      Journal of Medical Genetics
    14. PEARSON PL; BARLOW AL; HULTEN M
      MULTIVALENT FORMATION ASSOCIATED WITH POLYPLOIDY IN HUMAN MALE MEIOSIS

      American journal of human genetics
    15. HULTEN M
      JUBILEE HUMAN-CHROMOSOMES

      Trends in genetics
    16. LARSSON M; HULTEN M; BLEKKAN EA; ANDERSSON B
      THE EFFECT OF REACTION CONDITIONS AND TIME ON STREAM ON THE COKE FORMED DURING PROPANE DEHYDROGENATION

      Journal of catalysis
    17. STACEY M; BENNETT MS; HULTEN M
      FISH ANALYSIS ON SPONTANEOUSLY ARISING MICRONUCLEI IN THE ICF SYNDROME

      Journal of Medical Genetics
    18. BANERJEE S; SMALLWOOD A; HULTEN M
      ATP-DEPENDENT REORGANIZATION OF HUMAN SPERM NUCLEAR CHROMATIN

      Journal of Cell Science
    19. RENWICK PJ; BIRLEY AJ; MCKEOWN CME; HULTEN M
      SOUTHERN ANALYSIS REVEALS A LARGE DELETION AT THE HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE LOCUS IN A PATIENT WITH LESCH-NYHAN SYNDROME

      Clinical genetics
    20. WALLIS YL; MACDONALD F; KEIGHLEY MRB; NEOPTOLEMOS JPN; HULTEN M; MORTON DG
      SOMATIC ADENOMATOUS POLYPOSIS-COLI GENE-MUTATIONS ARE IMPLICATED IN MALIGNANT TRANSFORMATION IN FAMILIAL ADENOMATOUS POLYPOSIS

      British Journal of Surgery
    21. RAYBOULD MC; BIRLEY AJ; HULTEN M
      MOLECULAR VARIATION OF THE HUMAN ELASTIN (ELN) GENE IN A NORMAL HUMAN-POPULATION

      Annals of Human Genetics
    22. BANERJEE S; HULTEN M
      SPERM NUCLEAR CHROMATIN TRANSFORMATIONS IN SOMATIC CELL-FREE-EXTRACTS

      Molecular reproduction and development
    23. WALLIS YL; MACDONALD F; HULTEN M; MORTON JEV; MCKEOWN CM; NEOPTOLEMOS JP; KEIGHLEY M; MORTON DG
      GENOTYPE-PHENOTYPE CORRELATION BETWEEN POSITION OF CONSTITUTIONAL APCGENE MUTATION AND CHRPE EXPRESSION IN FAMILIAL ADENOMATOUS POLYPOSIS

      Human genetics
    24. RAYBOULD MC; BIRLEY AJ; HULTEN M
      2 NEW POLYMORPHISMS IN THE HUMAN ELASTIN GENE (ELN)

      Human genetics
    25. HULTEN M
      CHIASMA FORMATION, CROSSING-OVER AND RECOMBINATION IN MEIOSIS

      Trends in genetics
    26. LINDSAY EA; GRILLO A; FERRERO GB; ROTH EJ; MAGENIS E; GROMPE M; HULTEN M; GOULD C; BALDINI A; ZOGHBI HY; BALLABIO A
      MICROPHTHALMIA WITH LINEAR SKIN DEFECTS (MLS) SYNDROME - CLINICAL, CYTOGENETIC, AND MOLECULAR CHARACTERIZATION

      American journal of medical genetics
    27. MORTON J; MORTON D; MACDONALD F; WALLIS Y; RINDL P; HAYDON J; CULLEN R; NEOPTOLEMOS J; KEIGHLEY M; HULTEN M; MCKEOWN C
      IMPROVED SCREENING FOR FAP - EXPERIENCE FROM THE WEST MIDLANDS FAP REGISTER

      Journal of Medical Genetics
    28. RAYBOULD MC; BIRLEY AJ; HULTEN M
      A BGL-I POLYMORPHISM IN THE HUMAN ELASTIN GENE (ELN)

      Clinical genetics
    29. RAYBOULD MC; BIRLEY AJ; MOSS C; HULTEN M; MCKEOWN CME
      EXCLUSION OF AN ELASTIN GENE (ELN) MUTATION AS THE CAUSE OF PSEUDOXANTHOMA ELASTICUM (PXE) IN ONE FAMILY

      Clinical genetics
    30. HULTEN M; GOLDMAN A
      THE RELATIONSHIP BETWEEN MEIOTIC CHROMOSOME-PAIRING AND CHIASMA FORMATION

      Human genetics
    31. LAWRENCE S; COLLINS A; KEATS BJ; HULTEN M; MORTON NE
      INTEGRATION OF GENE MAPS - CHROMOSOME-21

      Proceedings of the National Academy of Sciences of the United Statesof America
    32. MARTIN RH; HULTEN M
      CHROMOSOME COMPLEMENTS IN 695 SPERM FROM 3 MEN HETEROZYGOUS FOR RECIPROCAL TRANSLOCATIONS, AND A REVIEW OF THE LITERATURE

      Hereditas


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 04/12/20 alle ore 19:47:22