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Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe.
Dörk, T; Macek, M; Mekus, F; Tümmler, B; Tzountzouris, J; Casals, T; Krebsová, A; Koudová, M; Sakmaryová, I; Macek, M; Vávrová, V; Zemková, D; Ginter, E; Petrova, N V; Ivaschenko, T; Baranov, V; Witt, M; Pogorzelski, A; Bal, J; Zékanowsky, C; Wagner, K; Stuhrmann, M; Bauer, I; Seydewitz, H H; Neumann, T; Jakubiczka, S.
Affiliation
  • Dörk T; Institute of Human Genetics, Medical School Hannover, Germany. doerk.thilo@mh-hannover.de
Hum Genet ; 106(3): 259-68, 2000 Mar.
Article in En | MEDLINE | ID: mdl-10798353
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Collection: 01-internacional Database: MEDLINE Main subject: Cystic Fibrosis Transmembrane Conductance Regulator / Cystic Fibrosis Limits: Child / Child, preschool / Female / Humans / Infant / Male / Newborn Country/Region as subject: Europa Language: En Journal: Hum Genet Year: 2000 Document type: Article Affiliation country:
Search on Google
Add to My VHL
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Cystic Fibrosis Transmembrane Conductance Regulator / Cystic Fibrosis Limits: Child / Child, preschool / Female / Humans / Infant / Male / Newborn Country/Region as subject: Europa Language: En Journal: Hum Genet Year: 2000 Document type: Article Affiliation country: