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    • Spina Bifida & other Dysraphisms (WG13)
    • Fetal medicine and pathology (WG6)
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    • Guidelines & consensus (WG11)
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    • ERN ITHACA Guidelines
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    • MOOC “bioinformatics”
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    • SysNDD Database
    • Training exchanges
    • Documentation for patients
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Home > Our Research Activities > List Of Publications > Stickler syndrome in the Czech Republic: phenotypic variability and genetic heterogeneity

Stickler syndrome in the Czech Republic: phenotypic variability and genetic heterogeneity

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Speech Perception and Production in Cochlear Implant Recipients with Pendred Syndrome
Monozygotic twins with Legius syndrome and differential diagnosis of Legius syndrome and neurof bromatosis type 1
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