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pro vyhledávání: '"Jacobé Dubs"'
Autor:
Patricia Dubot, Jing Liang, Jacobé Dubs, Yohann Missiak, Cédric Sarazin, François Couderc, Elizabeth Caussé
Publikováno v:
Practical Laboratory Medicine, Vol 13, Iss , Pp - (2019)
Background: Cystic fibrosis (CF) is the less rare and severe genetic disease among the European population. Biochemical diagnosis of CF is based on the demonstration of increased chloride concentration in sweat samples, obtained during the sweat test
Externí odkaz:
https://doaj.org/article/c55dfeb5d8f04a86862fbd2707ac08c9
Autor:
Jacobé Dubs, Jing Liang, François Couderc, Cédric Sarazin, Patricia Dubot, E Caussé, Yohann Missiak
Publikováno v:
Practical Laboratory Medicine
Practical Laboratory Medicine, Elsevier, 2019, 13, pp.e00114. ⟨10.1016/j.plabm.2018.e00114⟩
Practical Laboratory Medicine, 2019, 13, pp.e00114. ⟨10.1016/j.plabm.2018.e00114⟩
Practical Laboratory Medicine, Vol 13, Iss, Pp-(2019)
Practical Laboratory Medicine, Elsevier, 2019, 13, pp.e00114. ⟨10.1016/j.plabm.2018.e00114⟩
Practical Laboratory Medicine, 2019, 13, pp.e00114. ⟨10.1016/j.plabm.2018.e00114⟩
Practical Laboratory Medicine, Vol 13, Iss, Pp-(2019)
Background: Cystic fibrosis (CF) is the less rare and severe genetic disease among the European population. Biochemical diagnosis of CF is based on the demonstration of increased chloride concentration in sweat samples, obtained during the sweat test