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PATIENT
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Věra Kebrdlová
Person without affiliation with CUNI
59 publications
Publications
publication
Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families
2013 |
First Faculty of Medicine
publication
SHOX gene defects and selected dysmorphic signs in patients of idiopathic short stature and Léri-Weill dyschondrosteosis
2012 |
Faculty of Science, First Faculty of Medicine
publication
SHOX gene defects and selected dysmorphic signs in patients of idiopathic short stature and Leri-Weill dyschondrosteosis
2012 |
First Faculty of Medicine
publication
The Number of CAG Repeats Within the Normal Allele Does Not Influence the Age of Onset in Huntington's Disease
2011 |
First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Molecular genetic investigation of polymorfisms and STR loci in patients with nonsmall cell lung cancer
2009 |
First Faculty of Medicine
publication
New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease
2009 |
First Faculty of Medicine
publication
Huntington's Disease: Experience with Genetic Testing within 1994-2005
2007 |
First Faculty of Medicine
publication
Mutation analysis of the MYH gene in unrelated Czech APC mutation-negative polyposis patients
2007 |
First Faculty of Medicine
publication
PAR1 deletion/duplication in patients with dyschondrosteosis or idiopathic short stature
Publication without faculty affiliation
publication
Complex genetic analysis of SHOX gene in patients with dyschondrosteosis or idiopathic short stature
Publication without faculty affiliation
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