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M Koudová

Showing results (1-10 of 7) with videos related to

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Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|September 22, 2009
[Hereditary pancreatitis]M Koudová, R Kotalová, J Spicák, et al.
Casopis Lekaru Ceskych|April 4, 2000
[Cystic fibrosis--a disease of adolescents and adults?]V Vávrová, D Zemková, J Bartosová, et al.
Human Genetics|May 8, 2000
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 EuropeT Dörk, M Macek, F Mekus, et al.
Casopis Lekaru Ceskych|March 20, 2002
[Medical genetics in reproductive medicine]M Macek, S Vilímová, P Potuzníková, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|August 22, 2024
The guidelines for clinical practice for carriers of germline mutations in hereditary breast, ovarian, prostate, and pancreatic cancer predisposition genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 (4.2024)P Kleiblová, J Novotný, D Cibula, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|November 8, 2024
The guidelines for clinical practice for carriers of germline mutations in the Lynch syndrome predisposition genes MLH1, MSH2, MSH6, PMS2 and large deletions of EPCAM (4.2024)J Novotný, D Cibula, V Curtisová, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|May 25, 2026
Reporting framework in the testing of predisposition to common adult solid tumors using next-generation sequencingJ Soukupová, M Koudová, L Foretová, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|September 22, 2009
[Hereditary pancreatitis]M Koudová, R Kotalová, J Spicák, et al.
Casopis Lekaru Ceskych|April 4, 2000
[Cystic fibrosis--a disease of adolescents and adults?]V Vávrová, D Zemková, J Bartosová, et al.
Human Genetics|May 8, 2000
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 EuropeT Dörk, M Macek, F Mekus, et al.
Casopis Lekaru Ceskych|March 20, 2002
[Medical genetics in reproductive medicine]M Macek, S Vilímová, P Potuzníková, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|August 22, 2024
The guidelines for clinical practice for carriers of germline mutations in hereditary breast, ovarian, prostate, and pancreatic cancer predisposition genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 (4.2024)P Kleiblová, J Novotný, D Cibula, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|November 8, 2024
The guidelines for clinical practice for carriers of germline mutations in the Lynch syndrome predisposition genes MLH1, MSH2, MSH6, PMS2 and large deletions of EPCAM (4.2024)J Novotný, D Cibula, V Curtisová, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|May 25, 2026
Reporting framework in the testing of predisposition to common adult solid tumors using next-generation sequencingJ Soukupová, M Koudová, L Foretová, et al.
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