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E Feráková

Showing results (1-10 of 9) with videos related to

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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.
Human Heredity|February 17, 1998
Linkage of autosomal recessive primary congenital glaucoma to the GLC3A locus in Roms (Gypsies) from SlovakiaM Plásilová, E Feráková, L Kádasi, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|August 1, 1994
Distribution of ApoBII, MCT118 (D1S80), YNZ22 (D17S30), and COL2A1 Amp-FLPs (amplified fragment length polymorphisms) in Caucasoid population of SlovakiaL Kádasi, J Gécz, I Feráková, et al.
General Physiology and Biophysics|February 19, 2008
Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from SlovakiaI Zmetáková, V Ferák, G Minárik, et al.
General Physiology and Biophysics|July 31, 2007
Detection of His1069Gln mutation in Wilson disease by bidirectional PCR amplification of specific alleles (BI-PASA) testH Poláková, B Katrincsáková, G Minárik, et al.
Bratislavske Lekarske Listy|April 1, 1994
[DNA analysis in classic phenylketonuria--screening for mutations and haplotype analysis in Slovak families]L Kádasi, H Poláková, E Feráková, et al.
Human Genetics|January 1, 1995
PKU in Slovakia: mutation screening and haplotype analysisL Kádasi, H Poláková, E Feráková, et al.
American Journal of Human Genetics|October 6, 2000
High frequency of alkaptonuria in Slovakia: evidence for the appearance of multiple mutations in HGO involving different mutational hot spotsA Zatková, D B de Bernabé, H Poláková, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
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.
Human Heredity|February 17, 1998
Linkage of autosomal recessive primary congenital glaucoma to the GLC3A locus in Roms (Gypsies) from SlovakiaM Plásilová, E Feráková, L Kádasi, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|August 1, 1994
Distribution of ApoBII, MCT118 (D1S80), YNZ22 (D17S30), and COL2A1 Amp-FLPs (amplified fragment length polymorphisms) in Caucasoid population of SlovakiaL Kádasi, J Gécz, I Feráková, et al.
General Physiology and Biophysics|February 19, 2008
Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from SlovakiaI Zmetáková, V Ferák, G Minárik, et al.
General Physiology and Biophysics|July 31, 2007
Detection of His1069Gln mutation in Wilson disease by bidirectional PCR amplification of specific alleles (BI-PASA) testH Poláková, B Katrincsáková, G Minárik, et al.
Bratislavske Lekarske Listy|April 1, 1994
[DNA analysis in classic phenylketonuria--screening for mutations and haplotype analysis in Slovak families]L Kádasi, H Poláková, E Feráková, et al.
Human Genetics|January 1, 1995
PKU in Slovakia: mutation screening and haplotype analysisL Kádasi, H Poláková, E Feráková, et al.
American Journal of Human Genetics|October 6, 2000
High frequency of alkaptonuria in Slovakia: evidence for the appearance of multiple mutations in HGO involving different mutational hot spotsA Zatková, D B de Bernabé, H Poláková, et al.
Pageof 1