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Joubert Syndrome is a rare, autosomal recessive AR disorder characterized byneurologic findings as hypotonia, ataxia, physhcomotor developmental delay, abnormal respiratory pattern and abnormal eye movements. Molar tooth sign caused by cerebellar ver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95ba00e687fc43f0dc1d13e7879bd705
https://hdl.handle.net/11443/475
https://hdl.handle.net/11443/475
