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La ricerca find articoli where authors phrase all words ' Bonne-Tamir, B' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 17 riferimenti
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    1. Scott, HS; Kudoh, J; Wattenhofer, M; Shibuya, K; Berry, A; Chrast, R; Guipponi, M; Wang, J; Kawasaki, K; Asakawa, S; Minoshima, S; Younus, F; Mehdi, SQ; Radhakrishna, U; Papasavvas, MP; Gehrig, C; Rossier, C; Korostishevsky, M; Gal, A; Shimizu, N; Bonne-Tamir, B; Antonarakis, SE
      Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

      NATURE GENETICS
    2. Wattenhofer, M; Shibuya, K; Kudoh, J; Lyle, R; Michaud, J; Rossier, C; Kawasaki, K; Asakawa, S; Minoshima, S; Berry, A; Bonne-Tamir, B; Shimizu, N; Antonarakis, SE; Scott, HS
      Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domains

      HUMAN GENETICS
    3. Rosenberg, NA; Woolf, E; Pritchard, JK; Schaap, T; Gefel, D; Shpirer, I; Lavi, U; Bonne-Tamir, B; Hillel, J; Feldman, MW
      Distinctive genetic signatures in the Libyan Jews

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    4. Ben-Yosef, T; Wattenhofer, M; Riazuddin, S; Ahmed, ZM; Scot, HS; Kudoh, J; Shibuya, K; Antonarakis, SE; Bonne-Tamir, B; Radhakrishna, U; Naz, S; Ahmed, Z; Riazuddin, S; Pandya, A; Nance, WE; Wilcox, ER; Friedman, TB; Morell, RJ
      Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness

      JOURNAL OF MEDICAL GENETICS
    5. Mateu, E; Calafell, F; Lao, O; Bonne-Tamir, B; Kidd, JR; Pakstis, A; Kidd, KK; Bertranpetit, J
      Worldwide genetic analysis of the CFTR region

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. Underhill, PA; Shen, PD; Lin, AA; Jin, L; Passarino, G; Yang, WH; Kauffman, E; Bonne-Tamir, B; Bertranpetit, J; Francalacci, P; Ibrahim, M; Jenkins, T; Kidd, JR; Mehdi, SQ; Seielstad, MT; Wells, RS; Piazza, A; Davis, RW; Feldman, MW; Cavalli-Sforza, LL; Oefner, PJ
      Y chromosome sequence variation and the history of human populations

      NATURE GENETICS
    7. Adato, A; Raskin, L; Petit, C; Bonne-Tamir, B
      Deafness heterogeneity in a Druze isolate from the Middle East: novel OTOFand PDS mutations, low prevalence of GJB2 35delG mutation and indication for a new DFNB locus

      EUROPEAN JOURNAL OF HUMAN GENETICS
    8. Bartoloni, T; Wattenhofer, M; Kudoh, J; Berry, A; Shibuya, K; Kawasaki, K; Wang, J; Asakawa, S; Talior, I; Bonne-Tamir, B; Rossier, C; Michaud, J; McCabe, ERB; Minoshima, S; Shimizu, N; Scott, HS; Antonarakis, SE
      Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 ou G3PP) on 21q22.3: Mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase deficiency

      GENOMICS
    9. Berry, A; Scott, HS; Kudoh, J; Talior, I; Korostishevsky, M; Wattenhofer, M; Guipponi, M; Barras, C; Rossier, C; Shibuya, K; Wang, J; Kawasaki, K; Asakawa, S; Minoshima, S; Shimizu, N; Antonarakis, S; Bonne-Tamir, B
      Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region

      GENOMICS
    10. Michaud, J; Kudoh, J; Berry, A; Bonne-Tamir, B; Lalioti, MD; Rossier, C; Shibuya, K; Kawasaki, K; Asakawa, S; Minoshima, S; Shimizu, N; Antonarakis, SE; Scott, HS
      Isolation and characterization of a human chromosome 21q22.3 gene (WDR4) and its mouse homologue that code for a WD-repeat protein

      GENOMICS
    11. Hammer, MF; Redd, AJ; Wood, ET; Bonner, MR; Jarjanazi, H; Karafet, T; Santachiara-Benerecetti, S; Oppenheim, A; Jobling, MA; Jenkins, T; Ostrer, H; Bonne-Tamir, B
      Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    12. Kidd, JR; Pakstis, AJ; Zhao, HY; Lu, RB; Okonofua, FE; Odunsi, A; Grigorenko, E; Bonne-Tamir, B; Friedlaender, J; Schulz, LO; Parnas, J; Kidd, KK
      Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations

      AMERICAN JOURNAL OF HUMAN GENETICS
    13. Amar, A; Kwon, OJ; Motro, U; Witt, CS; Bonne-Tamir, B; Gabison, R; Brautbar, C
      Molecular analysis of HLA class II polymorphisms among different ethnic groups in Israel

      HUMAN IMMUNOLOGY
    14. Amar, A; Brautbar, C; Motro, U; Fisher, T; Bonne-Tamir, B; Israel, S
      Genetic variation of three tetrameric tandem repeats in four distinct Israeli ethnic groups

      JOURNAL OF FORENSIC SCIENCES
    15. Adato, A; Kalinski, H; Weil, D; Chaib, H; Korostishevsky, M; Bonne-Tamir, B
      Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance

      AMERICAN JOURNAL OF HUMAN GENETICS
    16. Macaulay, V; Richards, M; Hickey, E; Vega, E; Cruciani, F; Guida, V; Scozzari, R; Bonne-Tamir, B; Sykes, B; Torroni, A
      The emerging tree of west Eurasian mtDNAs: A synthesis of control-region sequences and RFLPs

      AMERICAN JOURNAL OF HUMAN GENETICS
    17. Mateu, E; Calafell, F; Bonne-Tamir, B; Kidd, JR; Casals, T; Kidd, KK; Bertranpetit, J
      Allele frequencies in a worldwide survey of a CA repeat in the first intron of the CFTR gene

      HUMAN HEREDITY


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/01/21 alle ore 14:22:10