AAAAAA

   
Results: 1-8 |
Results: 8
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females
Authors: 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
Citation: M. Vacca et al., Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females, J MOL MED-J, 78(11), 2001, pp. 648
Guidelines for reporting clinical features in cases with MECP2 mutations
Authors: 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
Citation: Am. Kerr et al., Guidelines for reporting clinical features in cases with MECP2 mutations, BRAIN DEVEL, 23(4), 2001, pp. 208-211
Non-invasive prenatal diagnosis of Down's syndrome
Authors: Hulten, M
Citation: M. Hulten, Non-invasive prenatal diagnosis of Down's syndrome, LANCET, 357(9260), 2001, pp. 963-964
Mammalian meiotic telomeres: Protein composition and redistribution in relation to nuclear pores
Authors: Scherthan, H Jerratsch, M Li, BB Smith, S Hulten, M Lock, T de Lange, T
Citation: H. Scherthan et al., Mammalian meiotic telomeres: Protein composition and redistribution in relation to nuclear pores, MOL BIOL CE, 11(12), 2000, pp. 4189-4203
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location
Authors: 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
Citation: Jp. Cheadle et al., Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location, HUM MOL GEN, 9(7), 2000, pp. 1119-1129
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)
Authors: 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
Citation: Jp. Cheadle et al., 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), HUM MOL GEN, 9(11), 2000, pp. 1717-1717
The compression/absorption cycle - influence of some major parameters on COP and a comparison with the compression cycle
Authors: Hulten, M Berntsson, T
Citation: M. Hulten et T. Berntsson, The compression/absorption cycle - influence of some major parameters on COP and a comparison with the compression cycle, INT J REFR, 22(2), 1999, pp. 91-106
Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene
Authors: Xu, GL Bestor, TH Bourc'his, D Hsieh, CL Tommerup, N Bugge, M Hulten, M Qu, XY Russo, JJ Viegas-Pequignot, E
Citation: Gl. Xu et al., Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene, NATURE, 402(6758), 1999, pp. 187-191
Risultati: 1-8 |