Detalhe da pesquisa
1.
Cystic fibrosis in Afro-Brazilians: XK haplotypes analysis supports the European origin of p.F508del mutation.
Genetica
; 145(1): 19-25, 2017 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-28160168
2.
p.Phe508del, p.Gly542X, p.Arg1162X, p.Asn1303Lys, and p.Lys683serfsX38 mutations in CF newborn screening of Brazilian children.
Clin Genet
; 92(1): 115-116, 2017 07.
Artigo
Inglês
| MEDLINE | ID: mdl-28134438
3.
Mannan-binding lectin MBL2 gene polymorphism in chronic hepatitis C: association with the severity of liver fibrosis and response to interferon therapy.
Clin Exp Immunol
; 152(2): 258-64, 2008 May.
Artigo
Inglês
| MEDLINE | ID: mdl-18336595
4.
Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling.
Andrology
; 6(1): 127-135, 2018 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29216686
5.
Cystic fibrosis in a southern Brazilian population: characteristics of 90% of the alleles.
Clin Genet
; 72(3): 218-23, 2007 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-17718859
6.
Cystic fibrosis gene variability in two southern Brazilian Amerindian populations: analysis of the deltaF508 mutation and the KM19 and XV2C haplotypes.
Hum Biol
; 79(1): 79-91, 2007 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-17985657
7.
Mannan-binding lectin plasma levels in leprosy: deficiency confers protection against the lepromatous but not the tuberculoid forms.
Clin Exp Immunol
; 145(3): 463-8, 2006 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-16907914