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common haplotype of protamine 1 and 2 genes is associated with higher sperm counts

International journal of andrology, 2010-02, Vol.33 (1), p.e240-e248

2010

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Association of Human Aging with a Functional Variant of Klotho

Proceedings of the National Academy of Sciences - PNAS, 2002-01, Vol.99 (2), p.856-861

2002

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Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survival

Human genetics, 1997-05, Vol.99 (5), p.565-572

1997

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P1107First results of molecular autopsy examinations in sudden cardiac death drawn from nationwide multidisciplinary and multicentric collaboration in the Czech Republic

Europace (London, England), 2020-06, Vol.22 (Supplement_1)

2020

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Size matters: Associations between the androgen receptor CAG repeat length and the intrafollicular hormone milieu

Molecular and cellular endocrinology, 2016-01, Vol.419, p.12-17

2016

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601Genetic testing identified arrhythmogenic cardiomyopathy with predominant left ventricular involvement in a cohort of patients with clinical diagnosis of familiar dilated cardiomyopathy

Europace (London, England), 2017-06, Vol.19 (suppl_3), p.iii126-iii126

2017

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An ADP-ribosyltransferase 3 (ART3) variant is associated with reducedsperm counts in Czech males: case/control association study replicating results from the Japanese population

Neuro-endocrinology letters, 2012-01, Vol.33 (1)

2012

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SCA2 trinucleotide expansion in German SCA patients

Neurogenetics, 1997-05, Vol.1 (1), p.59-64

1997

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Chromosome Y microdeletions in Czech men with severe reproductive disorders

Časopis lékařů českých, 2003, Vol.142 (11), p.670

2003

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Cystic fibrosis patients bearing both the common missense mutation Gly→Asp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes, except for decreased risk and meconium illeus

American journal of human genetics, 1992, Vol.51 (2), p.245-250

1992

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Sex determination using the polymerase chain reaction method for amplification of DNA segments on the X and Y chromosomes

Československá pediatrie, 1990-06, Vol.45 (6), p.323

1990

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Chromosome topology in normal and aneuploid blastomeres from human embryos

Prenatal diagnosis, 2007-12, Vol.27 (12), p.1091-1099

2007

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QF-PCR Examination of Parental and Meiotic Origin of Trisomy 21 in Central and Eastern Europe

The journal of histochemistry and cytochemistry, 2005-03, Vol.53 (3), p.371-373

2005

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Topology of Chromosomes 18 and X in Human Blastomeres from 3- to 4-Day-old Embryos

The journal of histochemistry and cytochemistry, 2005-03, Vol.53 (3), p.273-276

2005

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Possible association of the allele status of the CS.7/ Hha I polymorphism 5′ of the CFTR gene with postnatal female survival

Human genetics, 1997-04, Vol.99 (5), p.565-572

1997

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common haplotype of protamine 1 and 2 genes is associated with higher sperm counts

Association of Human Aging with a Functional Variant of Klotho

Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survival

P1107First results of molecular autopsy examinations in sudden cardiac death drawn from nationwide multidisciplinary and multicentric collaboration in the Czech Republic

Size matters: Associations between the androgen receptor CAG repeat length and the intrafollicular hormone milieu

601Genetic testing identified arrhythmogenic cardiomyopathy with predominant left ventricular involvement in a cohort of patients with clinical diagnosis of familiar dilated cardiomyopathy

An ADP-ribosyltransferase 3 (ART3) variant is associated with reducedsperm counts in Czech males: case/control association study replicating results from the Japanese population

SCA2 trinucleotide expansion in German SCA patients

Chromosome Y microdeletions in Czech men with severe reproductive disorders

Cystic fibrosis patients bearing both the common missense mutation Gly→Asp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes, except for decreased risk and meconium illeus

Sex determination using the polymerase chain reaction method for amplification of DNA segments on the X and Y chromosomes

Chromosome topology in normal and aneuploid blastomeres from human embryos

QF-PCR Examination of Parental and Meiotic Origin of Trisomy 21 in Central and Eastern Europe

Topology of Chromosomes 18 and X in Human Blastomeres from 3- to 4-Day-old Embryos

Possible association of the allele status of the CS.7/ Hha I polymorphism 5′ of the CFTR gene with postnatal female survival

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