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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 mucopolyssaccaridosis
T 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 family
C 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 Brazil
A 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 family
E 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 gene
G K Cury, U Matte, O Artigalás, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 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 mucopolyssaccaridosis
T 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 family
C 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 Brazil
A 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 family
E 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 gene
G K Cury, U Matte, O Artigalás, et al.
Page
of 1