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Preliminary study of haplotypes linked to the rare cystic fibrosis E1104X mutation.
Oueslati, S; Hadj Fredj, S; Belhaj, R; Siala, H; Bibi, A; Messaoud, Taieb.
Affiliation
  • Oueslati S; Children's Hospital Biochemistry Laboratory, Research Laboratory "Haemoglobinopathies and Cystic Fibrosis, LROOSPO3" Tunis Tunisia.
  • Hadj Fredj S; Children's Hospital Biochemistry Laboratory, Research Laboratory "Haemoglobinopathies and Cystic Fibrosis, LROOSPO3" Tunis Tunisia.
  • Belhaj R; Children's Hospital Biochemistry Laboratory, Research Laboratory "Haemoglobinopathies and Cystic Fibrosis, LROOSPO3" Tunis Tunisia.
  • Siala H; Children's Hospital Biochemistry Laboratory, Research Laboratory "Haemoglobinopathies and Cystic Fibrosis, LROOSPO3" Tunis Tunisia.
  • Bibi A; Children's Hospital Biochemistry Laboratory, Research Laboratory "Haemoglobinopathies and Cystic Fibrosis, LROOSPO3" Tunis Tunisia.
  • Messaoud T; Children's Hospital Biochemistry Laboratory, Research Laboratory "Haemoglobinopathies and Cystic Fibrosis, LROOSPO3" Tunis Tunisia.
Acta Physiol Hung ; 102(1): 86-93, 2015 Mar.
Article in En | MEDLINE | ID: mdl-25481366
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Haplotypes / Genetic Predisposition to Disease / Cystic Fibrosis Type of study: Prevalence_studies / Risk_factors_studies Limits: Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Africa Language: En Journal: Acta Physiol Hung Year: 2015 Type: Article
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Haplotypes / Genetic Predisposition to Disease / Cystic Fibrosis Type of study: Prevalence_studies / Risk_factors_studies Limits: Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Africa Language: En Journal: Acta Physiol Hung Year: 2015 Type: Article