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Anticancer Research
|
January 1, 1982
ATP uptake by mouse lymphoma cells
M F De Castro, S R Ayad
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
January 1, 1989
Cardiovascular change in response to prolonged defense area stimulation in freely moving rats
M F De Castro, L C Schenberg
Acta Anaesthesiologica Scandinavica
|
May 1, 1992
EDTA-dependent pseudothrombocytopenia in a preoperative patient
D Pestaña, C Marcote, M F de Castro
American Journal of Medical Genetics. Part A
|
December 8, 2006
Unusually severe expression of craniofacial features in Aarskog-Scott syndrome due to a novel truncating mutation of the FGD1 gene
A Orrico, L Galli, M G Obregon, et al.
Pediatrics
|
January 9, 2013
Change in prevalence of congenital defects in children with Prader-Willi syndrome
M Torrado, M E Foncuberta, M F de Castro Perez, et al.
Arquivos Brasileiros De Cardiologia
|
April 1, 1993
[Surgery for Wolff-Parkinson-White syndrome in the first year of life]
F A Fantini, E B Sternick, B Gontijo Filho, et al.
Journal of Community Genetics
|
August 2, 2013
CHACO outreach project: the development of a primary health care-based medical genetic service in an Argentinean province
C Z Barreiro, M P Bidondo, J A Garrido, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Anticancer Research
|
January 1, 1982
ATP uptake by mouse lymphoma cells
M F De Castro, S R Ayad
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
January 1, 1989
Cardiovascular change in response to prolonged defense area stimulation in freely moving rats
M F De Castro, L C Schenberg
Acta Anaesthesiologica Scandinavica
|
May 1, 1992
EDTA-dependent pseudothrombocytopenia in a preoperative patient
D Pestaña, C Marcote, M F de Castro
American Journal of Medical Genetics. Part A
|
December 8, 2006
Unusually severe expression of craniofacial features in Aarskog-Scott syndrome due to a novel truncating mutation of the FGD1 gene
A Orrico, L Galli, M G Obregon, et al.
Pediatrics
|
January 9, 2013
Change in prevalence of congenital defects in children with Prader-Willi syndrome
M Torrado, M E Foncuberta, M F de Castro Perez, et al.
Arquivos Brasileiros De Cardiologia
|
April 1, 1993
[Surgery for Wolff-Parkinson-White syndrome in the first year of life]
F A Fantini, E B Sternick, B Gontijo Filho, et al.
Journal of Community Genetics
|
August 2, 2013
CHACO outreach project: the development of a primary health care-based medical genetic service in an Argentinean province
C Z Barreiro, M P Bidondo, J A Garrido, et al.
Page
of 1