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Human Genetics|January 1, 1982
Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onsetA Gencik, A Gencikova, V FerákHuman Genetics|January 1, 1982
Population genetic aspects of primary congenital glaucoma. II. Fitness, parental consanguinity, founder effectV Ferák, A Gencik, A GencikovaCeska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|November 18, 1998
[Molecular diagnosis of mutations responsible for recurrent and severe forms of primary congenital glaucoma]M Plásilová, A Gerinec, V FerákZeitschrift Fur Alternsforschung|January 1, 1976
[Y-chromatin frequency, age (author's transl)]H Paláková, V Ferák, A GenĕíkJournal of Perinatal Medicine|January 1, 1980
Y chromatin frequency in white blood cells of newborn malesH Poláková, A Gencík, V FerákCeska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|November 18, 1998
[2 clinico-genetic types of primary congenital glaucomas in Slovakia]A Gerinec, V Ferák, M PlásilováBratislavske Lekarske Listy|March 1, 1990
[Use of DNA analysis in the diagnosis and prevention of hemophilia A]J Gécz, L Kádasi, H Poláková, et al.Ceskoslovenska Neurologie a Neurochirurgie|May 1, 1989
[Genetic linkage of the autosomal dominant form of Charcot-Marie-Tooth amyotrophy and 3 genetic markers on chromosome 1]V Ferák, L Kádasi, M Hrubisko, et al.Journal of Medical Genetics|May 5, 1999
Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucomaM Plásilová, I Stoilov, M Sarfarazi, et al.General Physiology and Biophysics|April 29, 2004
High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL)G Minárik, V Ferák, E Feráková, et al.Pageof 2