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pro vyhledávání: '"Mahmoud Ahmed Galal"'
Autor:
Muzammil Hafeez, Mahmoud Ahmed Galal, Anwar Khan, Gururaj Aithala Kodavooru, Hussein Z Adamjee Burhani, Yaser Husain Morsy El Saba, Rashid Mustafa, Manal Zaki Younis
Publikováno v:
Hamdan Medical Journal, Vol 13, Iss 4, Pp 235-238 (2020)
Joubert syndrome (OMIM 213300) is an uncommon autosomal recessive disorder that is characterised by distinct mid-hindbrain abnormalities, hypotonia and developmental delay. The molar tooth sign is a distinctive radiological feature of Joubert Syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::77736f4b9a6bd98e8c01a2122707bb16
http://www.hamdanjournal.org/article.asp?issn=2227-2437
http://www.hamdanjournal.org/article.asp?issn=2227-2437
