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Polar body array CGH for prediction of the status of the corresponding oocyte. Part I: clinical results

Human reproduction (Oxford), 2011-11, Vol.26 (11), p.3173-3180

2011

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ESHRE PGD Consortium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010

Human reproduction (Oxford), 2014-05, Vol.29 (5), p.880-903

2014

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What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium steering committee

Human reproduction (Oxford), 2010-04, Vol.25 (4), p.821-823

2010

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Intergeneric hybrid origin of the invasive tetraploid Cirsium vulgare

Plant biology (Stuttgart, Germany), 2024-08, Vol.26 (5), p.749-763

2024

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ESHRE PGD consortium best practice guidelines for fluorescence in situ hybridization-based PGD

Human reproduction (Oxford), 2011-01, Vol.26 (1), p.25-32

2011

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ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004

Human reproduction (Oxford), 2007-02, Vol.22 (2), p.323-336

2007

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Accreditation of the PGD laboratory

Human reproduction (Oxford), 2010-04, Vol.25 (4), p.1051-1065

2010

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ESHRE PGD Consortium data collection V: Cycles from January to December 2002 with pregnancy follow-up to October 2003

Human reproduction (Oxford), 2006-01, Vol.21 (1), p.3-21

2006

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Relocalization of Izumo and beta1-integrin during spontaneous acrosome reaction

Journal of reproductive immunology, 2012-05, Vol.94 (1), p.76-76

2012

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Lack of PAX4 mutations in 53 Czech MODYX families

Diabetic medicine, 2010-12, Vol.27 (12), p.1459-1460

2010

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36 Pre-hospital resuscitation of children in the city of prague

BMJ open, 2018-04, Vol.8 (Suppl 1), p.A13-A14

2018

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35 No gender differences found in bystander CPR in prague

BMJ open, 2018-04, Vol.8 (Suppl 1), p.A13-A13

2018

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SURF1 missense mutations promote a mild Leigh phenotype

Clinical genetics, 2009-08, Vol.76 (2), p.195-204

2009

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A new case of ALG8 deficiency (CDG Ih)

Journal of inherited metabolic disease, 2009-12, Vol.32 (Suppl 1), p.259-264

2009

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Mutations in genes affecting fertility of men - current routine laboratory genetic diagnostics and searching for more DNA segments and genes influencing spermatogenesis

Ceská gynekologie, 2016, Vol.81 (6), p.437

2016

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15. THE INCIDENCE AND ORIGIN OF CHROMOSOME ANEUPLOIDIES IN HIGH QUALITY KARYOMAPPING SNP PROFILES

Reproductive biomedicine online, 2019-08, Vol.39, p.e24-e24

2019

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SEVEN CASES OF CHROMOSOMAL MOSAICISM PERSISTING THROUGH GESTATION: CLINICAL IMPLICATIONS AND RECOMMENDATIONS FOR PRENATAL TESTING

Fertility and sterility, 2024-07, Vol.122 (1), p.e8-e8

2024

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What can karyomapping teach us about segmental mosaicism and mechanisms of its origin

Reproductive biomedicine online, 2019-04, Vol.38, p.e18-e19

2019

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26. MAJOR FACTORS INVOLVING AN IMPLANTATION RATE OF PGT-A EUPLOID EMBRYOS IN EGG DONATION PROGRAM OVER 35 YEARS

Reproductive biomedicine online, 2019-08, Vol.39, p.e42-e43

2019

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Polar body array CGH for prediction of the status of the corresponding oocyte. Part II: technical aspects

Human reproduction (Oxford), 2011-11, Vol.26 (11), p.3181-3185

2011

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Non-invasive fetal RHD and RHCE genotyping from maternal plasma in alloimmunized pregnancies

Prenatal diagnosis, 2005-12, Vol.25 (12), p.1079-1083

2005

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OP05.04: Non‐invasive diagnosis of RhD status and fetal gender from maternal plasma: our results from years 2008 to 2014

Ultrasound in obstetrics & gynecology, 2015-09, Vol.46 (S1), p.66-66

2015

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Plasma Cysteine Concentrations in Uncomplicated Pregnancies

Fetal diagnosis and therapy, 2007-01, Vol.22 (4), p.254-258

2007

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Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1

Biochemical journal, 2005-12, Vol.392 (Pt 3), p.625-632

2005

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What next for preimplantation genetic screening?

Human reproduction (Oxford), 2008-03, Vol.23 (3), p.478-480

2008

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Polar body array CGH for prediction of the status of the corresponding oocyte. Part I: clinical results

ESHRE PGD Consortium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010

What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium steering committee

Intergeneric hybrid origin of the invasive tetraploid Cirsium vulgare

ESHRE PGD consortium best practice guidelines for fluorescence in situ hybridization-based PGD

ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004

Accreditation of the PGD laboratory

ESHRE PGD Consortium data collection V: Cycles from January to December 2002 with pregnancy follow-up to October 2003

Relocalization of Izumo and beta1-integrin during spontaneous acrosome reaction

Lack of PAX4 mutations in 53 Czech MODYX families

36 Pre-hospital resuscitation of children in the city of prague

35 No gender differences found in bystander CPR in prague

SURF1 missense mutations promote a mild Leigh phenotype

A new case of ALG8 deficiency (CDG Ih)

Mutations in genes affecting fertility of men - current routine laboratory genetic diagnostics and searching for more DNA segments and genes influencing spermatogenesis

15. THE INCIDENCE AND ORIGIN OF CHROMOSOME ANEUPLOIDIES IN HIGH QUALITY KARYOMAPPING SNP PROFILES

SEVEN CASES OF CHROMOSOMAL MOSAICISM PERSISTING THROUGH GESTATION: CLINICAL IMPLICATIONS AND RECOMMENDATIONS FOR PRENATAL TESTING

What can karyomapping teach us about segmental mosaicism and mechanisms of its origin

26. MAJOR FACTORS INVOLVING AN IMPLANTATION RATE OF PGT-A EUPLOID EMBRYOS IN EGG DONATION PROGRAM OVER 35 YEARS

Polar body array CGH for prediction of the status of the corresponding oocyte. Part II: technical aspects

Non-invasive fetal RHD and RHCE genotyping from maternal plasma in alloimmunized pregnancies

OP05.04: Non‐invasive diagnosis of RhD status and fetal gender from maternal plasma: our results from years 2008 to 2014

Plasma Cysteine Concentrations in Uncomplicated Pregnancies

Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1

What next for preimplantation genetic screening?

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