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E R Valadares

Showing results (1-10 of 6) with videos related to

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Jornal De Pediatria|December 20, 2003
[Cutis laxa associated to cardiac failure]M F Siqueira, P A Ministério, E R Valadares, et al.
European Archives of Paediatric Dentistry : Official Journal of the European Academy of Paediatric Dentistry|February 2, 2020
Oral health of Brazilian individuals with mucopolyssaccaridosisT D Deps, E C França, E R Valadares, et al.
Genetics and Molecular Research : GMR|August 30, 2008
Mutation in intron 5 of GTP cyclohydrolase 1 gene causes dopa-responsive dystonia (Segawa syndrome) in a Brazilian familyC P Souza, E R Valadares, A L C Trindade, et al.
Genetics and Molecular Research : GMR|June 25, 2009
A985G mutation incidence in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in BrazilA C S Ferreira, M P A Orlandi, V C Oliveira, et al.
Genetics and Molecular Research : GMR|January 26, 2011
Novel exon nucleotide deletion causes adrenoleukodystrophy in a Brazilian familyE R Valadares, A L C Trindade, L R Oliveira, et al.
Gene|April 10, 2013
Mucolipidosis II and III alpha/beta in Brazil: analysis of the GNPTAB geneG K Cury, U Matte, O Artigalás, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Jornal De Pediatria|December 20, 2003
[Cutis laxa associated to cardiac failure]M F Siqueira, P A Ministério, E R Valadares, et al.
European Archives of Paediatric Dentistry : Official Journal of the European Academy of Paediatric Dentistry|February 2, 2020
Oral health of Brazilian individuals with mucopolyssaccaridosisT D Deps, E C França, E R Valadares, et al.
Genetics and Molecular Research : GMR|August 30, 2008
Mutation in intron 5 of GTP cyclohydrolase 1 gene causes dopa-responsive dystonia (Segawa syndrome) in a Brazilian familyC P Souza, E R Valadares, A L C Trindade, et al.
Genetics and Molecular Research : GMR|June 25, 2009
A985G mutation incidence in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in BrazilA C S Ferreira, M P A Orlandi, V C Oliveira, et al.
Genetics and Molecular Research : GMR|January 26, 2011
Novel exon nucleotide deletion causes adrenoleukodystrophy in a Brazilian familyE R Valadares, A L C Trindade, L R Oliveira, et al.
Gene|April 10, 2013
Mucolipidosis II and III alpha/beta in Brazil: analysis of the GNPTAB geneG K Cury, U Matte, O Artigalás, et al.
Pageof 1