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R Vrtel

Showing results (1-10 of 8) with videos related to

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Casopis Lekaru Ceskych|August 18, 2004
[Prospects and applications of innovated quantitative fluorescent PCR (IQF PCR) in analyses of genetic mosaics using gonosomal sequences]R Vodicka, R Vrtel, L Dusek, et al.
Casopis Lekaru Ceskych|March 9, 2006
[Prenatal diagnostics of tuberous sclerosis based on causal mutation knowledge]R Vrtel, R Vodicka, A Santavá, et al.
Ceska Gynekologie|September 8, 2006
[Rapid detection of most frequent chromosomal aneuploidies by the multiplex QF PCR method in the first trimester of pregnancy]D Vrbická, R Vodicka, R Vrtel, et al.
Casopis Lekaru Ceskych|March 9, 2006
[Analysis of free foetal DNA in maternal plasma using STR loci]R Vodicka, R Vrtel, M Procházka, et al.
Oncogene|November 15, 2016
Tumors overexpressing RNF168 show altered DNA repair and responses to genotoxic treatments, genomic instability and resistance to proteotoxic stressK Chroma, M Mistrik, P Moudry, et al.
Human Mutation|April 24, 1999
Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC) patients. Mutations in brief no. 119. OnlineQ Wang, S Verhoef, A M Tempelaars, et al.
Journal of Medical Genetics|January 1, 1996
Identification of a nonsense mutation at the 5' end of the TSC2 gene in a family with a presumptive diagnosis of tuberous sclerosis complexR Vrtel, S Verhoef, K Bouman, et al.
Casopis Lekaru Ceskych|March 9, 2006
[Frequency view on genome changes testing]R Brdicka, M Beránek, M Cimburová, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Casopis Lekaru Ceskych|August 18, 2004
[Prospects and applications of innovated quantitative fluorescent PCR (IQF PCR) in analyses of genetic mosaics using gonosomal sequences]R Vodicka, R Vrtel, L Dusek, et al.
Casopis Lekaru Ceskych|March 9, 2006
[Prenatal diagnostics of tuberous sclerosis based on causal mutation knowledge]R Vrtel, R Vodicka, A Santavá, et al.
Ceska Gynekologie|September 8, 2006
[Rapid detection of most frequent chromosomal aneuploidies by the multiplex QF PCR method in the first trimester of pregnancy]D Vrbická, R Vodicka, R Vrtel, et al.
Casopis Lekaru Ceskych|March 9, 2006
[Analysis of free foetal DNA in maternal plasma using STR loci]R Vodicka, R Vrtel, M Procházka, et al.
Oncogene|November 15, 2016
Tumors overexpressing RNF168 show altered DNA repair and responses to genotoxic treatments, genomic instability and resistance to proteotoxic stressK Chroma, M Mistrik, P Moudry, et al.
Human Mutation|April 24, 1999
Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC) patients. Mutations in brief no. 119. OnlineQ Wang, S Verhoef, A M Tempelaars, et al.
Journal of Medical Genetics|January 1, 1996
Identification of a nonsense mutation at the 5' end of the TSC2 gene in a family with a presumptive diagnosis of tuberous sclerosis complexR Vrtel, S Verhoef, K Bouman, et al.
Casopis Lekaru Ceskych|March 9, 2006
[Frequency view on genome changes testing]R Brdicka, M Beránek, M Cimburová, et al.
Pageof 1