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Search for publications relevant for "preimplantation genetic diagnosis"
preimplantation genetic diagnosis
Publication
Class
Person
Publication
Programmes
publication
Commentary: Preimplantation genetic diagnosis
2009 |
Second Faculty of Medicine
publication
Preimplantation genetic diagnosis and monogenic inherited eye diseases
2016 |
First Faculty of Medicine
publication
Repeated miscarriages in patients with antiphospholipid syndrome and subjected to in vitro fertilization: the importance of preimplantation genetic diagnosis
2012 |
Faculty of Medicine in Pilsen
publication
Commentary: Preimplantation Genetic Diagnosis
2009 |
First Faculty of Medicine
publication
Prerequisites for preimplantation genetic diagnosis (PGD in carriers of mutations responsible for hereditary cancers
2009 |
First Faculty of Medicine, Third Faculty of Medicine
publication
To assess the PGD results in couples with robertsonian and reciprocal translocations
2011 |
Third Faculty of Medicine, Central Library of Charles University
publication
Preimplantation Prenatal Diagnosis within the Framework of Reproductive Medicine and Rep-roductive Genetics
1999 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Single embryo transfer - possibilities and limits
2011 |
Third Faculty of Medicine
publication
Preimplantation genetic diagnostics of monogenic-based diseases: possibilities, pitfalls and first accomplishments in the Czech Republic
2008 |
Second Faculty of Medicine
publication
Current issues of assisted reproduction in the Czech Republic
2013 |
First Faculty of Medicine, Central Library of Charles University
publication
A rare Robertsonian translocation rob(14;22) carrier with azoospermia, meiotic defects, and testicular sperm aneuploidy
2015 |
Third Faculty of Medicine
publication
Gynecological Care and Prevention of Gynecological Malignancies in BRCA1 and BRCA2 Mutation Carriers
2016 |
First Faculty of Medicine
publication
Novel Splicing Variant in the PMM2 Gene in a Patient With PMM2-CDG Syndrome Presenting With Pericardial Effusion: A Case Report
2020 |
First Faculty of Medicine
publication
Molecular genetic cause of achromatopsia in two patients of Czech origin
2019 |
First Faculty of Medicine, Central Library of Charles University
publication
Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy
2013 |
Second Faculty of Medicine
publication
Clinical management of woman with bleeding disorders: A survey among European haemophilia treatment centres
2020 |
Publication without faculty affiliation