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M Havlovicová

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

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Casopis Lekaru Ceskych|September 20, 2002
[Genetics of autism]Z Sedlácek, M Havlovicová, M Hrdlicka
Casopis Lekaru Ceskych|March 20, 2002
[Specialized genetic counseling in pediatric and adult oncology patients]V Krutílková, M Havlovicová, P Goetz
Casopis Lekaru Ceskych|November 26, 2003
[Psychosocial factors associated with genetic testing for certain hereditary types of neoplasms]V Franková, J Zidovská, V Krutílková, et al.
Casopis Lekaru Ceskych|September 20, 2002
[Genetic study of 20 patients with autism disorders]M Havlovicová, L Propper, D Novotná, et al.
Casopis Lekaru Ceskych|March 25, 1998
[DNA diagnosis of the fragile X chromosome syndrome--FRAXA using PCR]A Bóday, V Mat'oska, V Konrádová, et al.
Casopis Lekaru Ceskych|December 9, 2004
[Case reports of patients with a marker chromosome]E Kocárek, D Novotná, T Maríková, et al.
Clinical Genetics|February 5, 2016
Molecular genetic analysis in 14 Czech Kabuki syndrome patients is confirming the utility of phenotypic scoringJ Paděrová, A Holubová, M Simandlová, et al.
Pageof 1

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

Sort By:
Pageof 1
Casopis Lekaru Ceskych|September 20, 2002
[Genetics of autism]Z Sedlácek, M Havlovicová, M Hrdlicka
Casopis Lekaru Ceskych|March 20, 2002
[Specialized genetic counseling in pediatric and adult oncology patients]V Krutílková, M Havlovicová, P Goetz
Casopis Lekaru Ceskych|November 26, 2003
[Psychosocial factors associated with genetic testing for certain hereditary types of neoplasms]V Franková, J Zidovská, V Krutílková, et al.
Casopis Lekaru Ceskych|September 20, 2002
[Genetic study of 20 patients with autism disorders]M Havlovicová, L Propper, D Novotná, et al.
Casopis Lekaru Ceskych|March 25, 1998
[DNA diagnosis of the fragile X chromosome syndrome--FRAXA using PCR]A Bóday, V Mat'oska, V Konrádová, et al.
Casopis Lekaru Ceskych|December 9, 2004
[Case reports of patients with a marker chromosome]E Kocárek, D Novotná, T Maríková, et al.
Clinical Genetics|February 5, 2016
Molecular genetic analysis in 14 Czech Kabuki syndrome patients is confirming the utility of phenotypic scoringJ Paděrová, A Holubová, M Simandlová, et al.
Pageof 1