ℹ️
🇬🇧
Search
Search for people relevant for "mutation rate"
mutation rate
Person
Class
Person
Publication
Programmes
Export current view
MUDr. Marie Glombová Ph.D.
External person at Second Faculty of Medicine
6 publications
Publications
publication
The importance of advanced parental age in the origin of neurofibromatosis type 1
2012 |
Second Faculty of Medicine
publication
Brain gliomas, hydrocephalus and idiopathic aqueduct stenosis in children with neurofibromatosis type 1
2019 |
Second Faculty of Medicine
publication
Neurofibromatosis von Recklinghausen type 1 (NF1) - the most common neurocutaneous disorder
2018 |
Second Faculty of Medicine
publication
Neurofibromatosis von Recklinghausen type 1 (NF1) - clinical picture and molecular-genetics diagnostic
2015 |
Second Faculty of Medicine, First Faculty of Medicine
publication
Homozygous EXOSC3 Mutation c.92G -> C, p.G31A is a Founder Mutation Causing Severe Pontocerebellar Hypoplasia Type 1 Among the Czech Roma
2013 |
Second Faculty of Medicine
publication
Idiopathic Aqueductal Stenosis and Developmental Speech Disorder in Children with Neurofibromatosis von Recklinghausen type 1-Two Case Reports
2012 |
Second Faculty of Medicine
Loading network view...