Search Results1-3 of  3

  • Santos Manuela ID: 9000326637821

    Articles in CiNii:1

    • New massive parallel sequencing approach improves the genetic characterization of congenital myopathies (2016)
  • SANTOS Manuela M. ID: 9000001952843

    Department of Medicine, CHUM, Universite de Montreal Hopital Notre-Dame (2006 from CiNii)

    Articles in CiNii:1

    • Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype (2006)
  • SANTOS Manuela ID: 9000018777335

    Servico de Neuropediatria, Hospital de Criancas Maria Pia (2011 from CiNii)

    Articles in CiNii:1

    • Rett syndrome with and without detected MECP2 mutations : An attempt to redefine phenotypes (2011)
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