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La ricerca find articoli where soggetti phrase all words 'non-disjunction' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 17 riferimenti
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    1. Honma, M; Momose, M; Sakamoto, H; Sofuni, T; Hayashi, M
      Spindle poisons induce allelic loss in mouse lymphoma cells through mitotic non-disjunction

      MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
    2. Bandyopadhyay, R; Berend, SA; Page, SL; Choo, KHA; Shaffer, LG
      Satellite III sequences on 14p and their relevance to Robertsonian translocation formation

      CHROMOSOME RESEARCH
    3. Minelli, A; Morerio, C; Maserati, E; Olivieri, C; Panarello, C; Bonvini, L; Leszl, A; Rosanda, C; Lanino, E; Danesino, C; Pasquali, F
      Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia

      LEUKEMIA
    4. Turner, JMA; Burgoyne, PS; Singh, PB
      M31 and macroH2A1.2 colocalise at the pseudoautosomal region during mouse meiosis

      JOURNAL OF CELL SCIENCE
    5. Thomas, NS; Collins, AR; Hassold, TJ; Jacobs, PA
      A reinvestigation of non-disjunction resulting in 47, XXY males of paternal origin

      EUROPEAN JOURNAL OF HUMAN GENETICS
    6. Jyothy, A; Kumar, KSD; Rao, GNM; Rao, VB; Swarna, M; Devi, BU; Sujatha, M; Kumari, CK; Reddy, PP
      Cytogenetic studies of 1001 Down syndrome cases from Andhra Pradesh, India

      INDIAN JOURNAL OF MEDICAL RESEARCH
    7. Amiel, A; Reish, O; Gaber, E; Kedar, I; Diukman, R; Fejgin, M
      Replication asynchrony increases in women at risk for aneuploid offspring

      CHROMOSOME RESEARCH
    8. Chen, CP; Chern, SR; Yeh, LF; Chen, WL; Chen, LF; Wang, W
      Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18

      PRENATAL DIAGNOSIS
    9. Chen, CP; Chern, SR; Chang, CL; Lee, CC; Chen, WL; Chen, LF; Wang, W
      Prenatal diagnosis and genetic analysis of X chromosome polysomy 49,XXXXY

      PRENATAL DIAGNOSIS
    10. DeLozier-Blanchet, CD; Roeder, E; Denis-Arrue, R; Blouin, JL; Low, J; Fisher, J; Scharnhorst, D; Curry, CJ
      Trisomy 12 mosaicism confirmed in multiple organs from a liveborn child

      AMERICAN JOURNAL OF MEDICAL GENETICS
    11. Robinson, WP; Christian, SL; Kuchinka, BD; Penaherrera, S; Das, S; Schuffenhauer, S; Malcolm, S; Schinzel, AA; Hassold, TJ; Ledbetter, DH
      Somatic segregation errors predominantly contribute to the gain or loss ofa paternal chromosome leading to uniparental disomy for chromosome 15

      CLINICAL GENETICS
    12. Gomez, D; Solsona, E; Guitart, M; Baena, N; Gabau, E; Egozcue, J; Caballin, MR
      Origin of trisomy 21 in Down syndrome cases from a Spanish population registry

      ANNALES DE GENETIQUE
    13. Honma, A; Ishii, R; Ito, A; Kato, M; Saitoh, S; Hayasaka, K
      Prader-Willi syndrome in a child with XYY

      JOURNAL OF HUMAN GENETICS
    14. Peschka, B; Leygraaf, J; van der Ven, K; Montag, M; Schartmann, B; Schubert, R; van der Ven, H; Schwanitz, G
      Type and frequency of chromosome aberrations in 781 couples undergoing intracytoplasmic sperm injection

      HUMAN REPRODUCTION
    15. Ballesta, F; Queralt, R; Gomez, D; Solsona, E; Guitart, M; Ezquerra, M; Moreno, J; Oliva, R
      Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21

      ANNALES DE GENETIQUE
    16. Lechniak, D; Switonski, M
      Aneuploidy in bovine oocytes matured in vitro

      CHROMOSOME RESEARCH
    17. TEASE C; FISHER G
      CYTOGENETIC AND GENETIC-STUDIES OF RADIATION-INDUCED CHROMOSOME-DAMAGE IN MOUSE OOCYTES .1. NUMERICAL AND STRUCTURAL CHROMOSOME-ANOMALIES IN METAPHASE-II OOCYTES, PREIMPLANTATION AND POSTIMPLANTATION EMBRYOS

      Mutation research


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Documento generato il 31/10/20 alle ore 01:56:36