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M F Coutinho

Showing results (21-30 of 25) with videos related to

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Bone and Mineral|June 1, 1988
Age-related changes in cancellous bone structure. A two-dimensional study in the transiliac and iliac crest biopsy sitesD H Birkenhäger-Frenkel, P Courpron, E A Hüpscher, et al.
Arquivos De Neuro-Psiquiatria|December 1, 1987
[Neurocryptococcosis in childhood. Report of 3 cases in the 1st decade of life]M H Fontana, M F Coutinho, E dos S Camargo, et al.
Clinical Genetics|January 26, 2008
Molecular analysis of mucopolysaccharidosis type IIIB in Portugal: evidence of a single origin for a common mutation (R234C) in the Iberian PeninsulaM Mangas, C Nogueira, M J Prata, et al.
Clinical Genetics|August 8, 2009
Molecular analysis of the GNPTAB and GNPTG genes in 13 patients with mucolipidosis type II or type III - identification of eight novel mutationsM Encarnação, L Lacerda, R Costa, et al.
Clinical Genetics|October 1, 2010
Origin and spread of a common deletion causing mucolipidosis type II: insights from patterns of haplotypic diversityM F Coutinho, M Encarnação, R Gomes, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Bone and Mineral|June 1, 1988
Age-related changes in cancellous bone structure. A two-dimensional study in the transiliac and iliac crest biopsy sitesD H Birkenhäger-Frenkel, P Courpron, E A Hüpscher, et al.
Arquivos De Neuro-Psiquiatria|December 1, 1987
[Neurocryptococcosis in childhood. Report of 3 cases in the 1st decade of life]M H Fontana, M F Coutinho, E dos S Camargo, et al.
Clinical Genetics|January 26, 2008
Molecular analysis of mucopolysaccharidosis type IIIB in Portugal: evidence of a single origin for a common mutation (R234C) in the Iberian PeninsulaM Mangas, C Nogueira, M J Prata, et al.
Clinical Genetics|August 8, 2009
Molecular analysis of the GNPTAB and GNPTG genes in 13 patients with mucolipidosis type II or type III - identification of eight novel mutationsM Encarnação, L Lacerda, R Costa, et al.
Clinical Genetics|October 1, 2010
Origin and spread of a common deletion causing mucolipidosis type II: insights from patterns of haplotypic diversityM F Coutinho, M Encarnação, R Gomes, et al.
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