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Detection of His1069Gln mutation in Wilson disease by bidirectional PCR amplification of specific alleles (BI-PASA) test

General physiology and biophysics, 2007-06, Vol.26 (2), p.91-96

2007

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Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma

Journal of medical genetics, 1999-04, Vol.36 (4), p.290-294

1999

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High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL)

General physiology and biophysics, 2003-12, Vol.22 (4), p.549

2003

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High Frequency of Alkaptonuria in Slovakia: Evidence for the Appearance of Multiple Mutations in HGO Involving Different Mutational Hot Spots

American journal of human genetics, 2000-11, Vol.67 (5), p.1333-1339

2000

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Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from Slovakia

General physiology and biophysics, 2007-12, Vol.26 (4), p.306-310

2007

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GJB2 gene mutations in Slovak hearing-impaired patients of Caucasian origin: spectrum, frequencies and SNP analysis

Clinical genetics, 2005-12, Vol.68 (6), p.554-557

2005

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Rapid detection methods for five HGO gene mutations causing alkaptonuria

Clinical genetics, 2003-02, Vol.63 (2), p.145-149

2003

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Linkage of Autosomal Recessive Primary Congenital Glaucoma to the GLC3A Locus in Roms (Gypsies) from Slovakia

Human heredity, 1998-01, Vol.48 (1), p.30-33

1998

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Novel mutations in the homogentisate- 1,2-dioxygenase gene identified in Slovak patients with alkaptonuria

Journal of medical genetics, 2000-07, Vol.37 (7), p.539-542

ZATKOVA, A

2000

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A unique RFLP haplotype at the phenylalanine hydroxylase locus in Czechoslovak Gypsies with phenylketonuria

Functional and developmental morphology, 1992, Vol.2 (2), p.139

1992

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Distribution of ApoBII, MCT118 (D1S80), YNZ22 (D17S30), and COL2A1 Amp-FLPs (amplified fragment length polymorphisms) in Caucasoid population of Slovakia

Gene geography : a computerized bulletin on human gene frequencies, 1994-08, Vol.8 (2), p.121

1994

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Dynamic mutation loci: allele distributions in different populations

Annals of human genetics, 1996-09, Vol.60 (5), p.391-400

1996

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DNA analysis in classic phenylketonuria--screening for mutations and haplotype analysis in Slovak families

Bratislavské lékarské listy, 1994-04, Vol.95 (4), p.147

1994

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Genetic diversity in widespread species is not congruent with species richness in alpine plant communities

Ecology letters, 2012-12, Vol.15 (12), p.1439-1448

2012

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new individual-based spatial approach for identifying genetic discontinuities in natural populations

Molecular ecology, 2007-05, Vol.16 (10), p.2031-2043

2007

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Some comments on the age-distribution of women with breast-cancer (author's transl)

Ceskoslovenska gynekologie, 1975-02, Vol.40 (1), p.27

1975

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Detection of His1069Gln mutation in Wilson disease by bidirectional PCR amplification of specific alleles (BI-PASA) test

Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma

High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL)

High Frequency of Alkaptonuria in Slovakia: Evidence for the Appearance of Multiple Mutations in HGO Involving Different Mutational Hot Spots

Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from Slovakia

GJB2 gene mutations in Slovak hearing-impaired patients of Caucasian origin: spectrum, frequencies and SNP analysis

Rapid detection methods for five HGO gene mutations causing alkaptonuria

Linkage of Autosomal Recessive Primary Congenital Glaucoma to the GLC3A Locus in Roms (Gypsies) from Slovakia

Novel mutations in the homogentisate- 1,2-dioxygenase gene identified in Slovak patients with alkaptonuria

A unique RFLP haplotype at the phenylalanine hydroxylase locus in Czechoslovak Gypsies with phenylketonuria

Distribution of ApoBII, MCT118 (D1S80), YNZ22 (D17S30), and COL2A1 Amp-FLPs (amplified fragment length polymorphisms) in Caucasoid population of Slovakia

Dynamic mutation loci: allele distributions in different populations

DNA analysis in classic phenylketonuria--screening for mutations and haplotype analysis in Slovak families

Genetic diversity in widespread species is not congruent with species richness in alpine plant communities

new individual-based spatial approach for identifying genetic discontinuities in natural populations

Some comments on the age-distribution of women with breast-cancer (author's transl)

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