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La ricerca find articoli where authors phrase all words ' van der Smagt, JJ' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 5 riferimenti
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    1. Bezrookove, V; Hansson, K; van der Burg, M; van der Smagt, JJ; Hilhorst-Hofstee, Y; Wiegant, J; Beverstock, GC; Raap, AK; Tanke, H; Breuning, MH; Rosenberg, C
      Individuals with abnormal phenotype and normal G-banding karyotype: improvement and limitations in the diagnosis by the use of 24-colour FISH

      HUMAN GENETICS
    2. van der Smagt, JJ; Beverstock, GC; Breuning, MH; Kanhai, HHH; Vandenbussche, FPHA
      Assessment of prenatal karyotypes

      HUMAN REPRODUCTION
    3. Petrij, F; Dauwerse, HG; Blough, RI; Giles, RH; van der Smagt, JJ; Wallerstein, R; Maaswinkel-Mooy, PD; van Karnebeek, CD; van Ommen, GJB; van Haeringen, A; Rubinstein, JH; Saal, HM; Hennekam, RCM; Peters, DJM; Breuning, MH
      Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations

      JOURNAL OF MEDICAL GENETICS
    4. Hes, FJ; McKee, S; Taphoorn, MJB; Rehal, P; van der Luijt, RB; McMahon, R; van der Smagt, JJ; Dow, D; Zewald, RA; Whittaker, J; Lips, CJM; MacDonald, F; Pearson, PL; Maher, ER
      Cryptic von Hippel-Lindau disease: germline mutations in patients with haemangioblastoma only

      JOURNAL OF MEDICAL GENETICS
    5. Brooks, AS; Breuning, MH; Osinga, J; Van der Smagt, JJ; Catsman, CE; Buys, CHCM; Meijers, C; Hofstra, RMW
      A consanguineous family with Hirschsprung disease, microcephaly, and mental retardation (Goldberg-Shprintzen syndrome)

      JOURNAL OF MEDICAL GENETICS


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 22/01/21 alle ore 20:31:56