Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Sangita, Mondol"'
Publikováno v:
Journal of pediatric hematology/oncology. 31(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba538aa1d997a122062be6af1b99b6e0
https://pubmed.ncbi.nlm.nih.gov/19770683
https://pubmed.ncbi.nlm.nih.gov/19770683
Publikováno v:
Journal of the Indian Medical Association. 105(7)
Joubert syndrome is a rare genetic disorder characterised by dysplasia of the cerebellar vermis and a malformed brainstem causing ataxia, tachypnoea, nystagmus, hypotonia and mental retardation. An early case of a two-month-old infant presenting with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ec96b562dc920e4bf085c46b9efe45a6
https://pubmed.ncbi.nlm.nih.gov/18178993
https://pubmed.ncbi.nlm.nih.gov/18178993