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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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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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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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Deep common ancestry of Indian and western-Eurasian mitochondrial DNA lineages

Current biology, 1999-11, Vol.9 (22), p.1331-1334

1999

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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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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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Correlation between Genotype and Phenotype in Patients with Cystic Fibrosis

The New England journal of medicine, 1993-10, Vol.329 (18), p.1308-1313

1993

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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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Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onset

Human genetics, 1982, Vol.61 (3), p.193-197

1982

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Lactase Haplotype Diversity in the Old World

American journal of human genetics, 2001-01, Vol.68 (1), p.160-172

2001

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Population genetic aspects of primary congenital glaucoma. II. Fitness, parental consanguinity, founder effect

Human genetics, 1982-10, Vol.61 (3), p.198-200

1982

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Haplotype analysis of the CFTR gene region and the proportion of delta F508 deletion in Slovak patients with cystic fibrosis

Functional and developmental morphology, 1992, Vol.2 (2), p.141

1992

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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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2 clinico-genetic types of primary congenital glaucomas in Slovakia

Česká a slovenská oftalmologie, 1998, Vol.54 (5), p.289

1998

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Molecular diagnosis of mutations responsible for recurrent and severe forms of primary congenital glaucoma

Česká a slovenská oftalmologie, 1998, Vol.54 (5), p.281

1998

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Deletion ΔF508 and haplotype analysis of CFTR gene region in Slovak CF patients

Human genetics, 1992-05, Vol.89 (3), p.305-306

1992

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Are population-genetic mechanisms responsible for clustering of cases of Creutzfeldt-Jakob disease?

British medical journal (Clinical research ed.), 1981-02, Vol.282 (6263), p.521

1981

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A probabilistic aspect of genetic determination of disputed paternity (author's transl)

Bratislavské lékarské listy, 1974-11, Vol.62 (5), p.584

1974

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Population-genetical characteristics of congenital glaucoma in Slovakia (author's transl)

Bratislavské lékarské listy, 1980-03, Vol.73 (3), p.295

1980

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Random and non-random component of inbreeding coefficient in localities with high incidence of alkaptonuria in Slovakia (author's transl)

Bratislavské lékarské listy, 1979-02, Vol.71 (2), p.144

1979

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Haptoglobin types in gypsies from Slovakia (Czechoslovakia)

Human heredity, 1969, Vol.19 (5), p.480

1969

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Recurrence risk figures for cleft lip and/or cleft palate (author's transl)

Bratislavské lékarské listy, 1978-03, Vol.69 (3), p.286

1978

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Analysis of some biological parameters in a population living within the effective range of a power station, concerning possible genetic risk (author's transl)

Bratislavské lékarské listy, 1977-01, Vol.67 (1), p.39

1977

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Interpopulation variability in gene frequencies between neighbouring villages (author's transl)

Bratislavské lékarské listy, 1979-11, Vol.72 (5), p.572

1979

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Genetic counseling

Bratislavské lékarské listy, 1973-02, Vol.59 (2), p.227

Ferák, V

1973

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

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

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

Deep common ancestry of Indian and western-Eurasian mitochondrial DNA lineages

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

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

Correlation between Genotype and Phenotype in Patients with Cystic Fibrosis

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

Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onset

Lactase Haplotype Diversity in the Old World

Population genetic aspects of primary congenital glaucoma. II. Fitness, parental consanguinity, founder effect

Haplotype analysis of the CFTR gene region and the proportion of delta F508 deletion in Slovak patients with cystic fibrosis

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

2 clinico-genetic types of primary congenital glaucomas in Slovakia

Molecular diagnosis of mutations responsible for recurrent and severe forms of primary congenital glaucoma

Deletion ΔF508 and haplotype analysis of CFTR gene region in Slovak CF patients

Are population-genetic mechanisms responsible for clustering of cases of Creutzfeldt-Jakob disease?

A probabilistic aspect of genetic determination of disputed paternity (author's transl)

Population-genetical characteristics of congenital glaucoma in Slovakia (author's transl)

Random and non-random component of inbreeding coefficient in localities with high incidence of alkaptonuria in Slovakia (author's transl)

Haptoglobin types in gypsies from Slovakia (Czechoslovakia)

Recurrence risk figures for cleft lip and/or cleft palate (author's transl)

Analysis of some biological parameters in a population living within the effective range of a power station, concerning possible genetic risk (author's transl)

Interpopulation variability in gene frequencies between neighbouring villages (author's transl)

Genetic counseling

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