ℹ️
🇬🇧
Search
Search for people relevant for "syndromu"
syndromu
Person
Class
Person
Publication
Programmes
MUDr. Markéta Havlovicová
Academic staff at Second Faculty of Medicine
95 publications
Publications
publication
Importance of Cerebral Folate Deficiency for Development and Treatment of Autism Spectrum Disorder
2014 |
Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Syndrome of the fragile x chromosome with Tremor/Ataxia (FXTAS): a pilot study in a group of patients with ataxia of unknown aetiology
2007 |
Second Faculty of Medicine
publication
Diagnostic possibilities of Prader-Willi and of Angelman syndromes
2005 |
Second Faculty of Medicine
publication
Prader-Willi Syndrome: Changes in Growth Dynamics and Body Composition during Treatment with Growth Hormone
2005 |
Second Faculty of Medicine
publication
Case report of patients with a marker chromosome
2004 |
Second Faculty of Medicine
publication
Genetic Study of Twenty Patients with Autism Spectrum Disorders
2002 |
Second Faculty of Medicine
publication
Relationship between Genotype and Phenotype in Patients with Microdeletion of Chromosome 22q11
2001 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Detection of Deletions and Uniparental Disomies in prade-Willi and Angelman Syndromes - Methodical and Interpretational Aspects
2000 |
Second Faculty of Medicine, Central Library of Charles University
publication
Detection of deletions and uniparental disomies in Prader-Willi and Angelman syndromes - methodical and interpretational aspects
2000 |
Second Faculty of Medicine
publication
DNA diagnosis of the fragile X chromosome syndrome - FRAXA using PCR
1998 |
Second Faculty of Medicine
Load more publications (85)
Loading network view...