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FOXL2
Person
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Person
Publication
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Miluše Prošková
Person without affiliation with CUNI
4 publications
Publications
publication
First cases in the Czech Republic of the Hallervorden-Spatz Disease resulting from mutation in the Pantothenate Kinase 2 Gene
+1
2005 |
Second Faculty of Medicine
publication
Pelizaeus Merzbacher's disease (PMD) - Detection of the most frequent mutation of the proteolipid protein gene in Czech patients and families with the classical form of PAID
2003 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Congenital muscular dystrophy with complete defect of merosine - First two cases confirmed in the Czech Republic - Typical phenotype and evidence based on skin biopsy
2002 |
Second Faculty of Medicine
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