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FREQUENCY OF THE CYSTIC-FIBROSIS DELTA-F-508 MUTATION IN A POPULATION FROM SAO-PAULO STATE, BRAZIL
(Assoc Bras Divulg CientificaSao PauloBrasil, 1993)
Molecular analysis of 23 exons of the cftr gene in brazilian patients leads to the finding of rare cystic fibrosis mutations
(Wayne State University Press, 2012)
Análise das prevalências de doenças detectadas pelo programa nacional de triagem neonatal no município de Araraquara no ano de 2009
(2011-11-14)
The National Neonatal Screening Program (NNSP) set up in all Brazil, aims, through planned phases of local implementation, to detect diseases such as phenylketonuria, congenital hypothyroidism, hemoglobinopathies and cystic ...
Análise das prevalências de doenças detectadas pelo programa nacional de triagem neonatal no município de Araraquara no ano de 2009
(2011-11-14)
The National Neonatal Screening Program (NNSP) set up in all Brazil, aims, through planned phases of local implementation, to detect diseases such as phenylketonuria, congenital hypothyroidism, hemoglobinopathies and cystic ...
Molecular analysis of 23 exons of the cftr gene in brazilian patients leads to the finding of rare cystic fibrosis mutations
(Wayne State University Press, 2005)
Genomovar status, virulence markers and genotyping of Burkholderia cepacia complex strains isolated from Brazilian cystic fibrosis patients
(ELSEVIER SCIENCE BV, 2008)
Burkholderia cepacia complex isolates obtained by microbiological culture of respiratory samples from Brazilian CF patients were studied by recA based PCR, screened by specific PCR for virulence markers and genotyped by ...