Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Iskandarani, Alaa I."'
Neuroblastoma amplified sequence gene mutation: A rare cause of recurrent liver failure in children.
Autor:
Hasosah, Mohammed Y.1 hasosah2007@yahoo.com, Iskandarani, Alaa I.1, Shawli, Ayman I.2, Alsahafi, Ashraf F.1, Sukkar, Ghassan A.1, Qurashi, Mansour A.3
Publikováno v:
Saudi Journal of Gastroenterology. May/Jun2017, Vol. 23 Issue 3, p206-208. 3p.
