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Prilozi|September 9, 2009
Type I Gaucher disease (GDI) in three siblings: enzyme replacement treatment (ERT) requiredZ S Gucev, V Tasic, N Pop-Jordanova, et al.Prilozi|January 31, 2012
Hunter syndrome (Muccopolysaccharridosis Type II) in Macedonia and BulgariaZ S Gucev, V Tasic, I Sinigerska, et al.Prilozi|January 31, 2012
Acute Gallbladder Hydrops and Arthritis: unusual initial manifestations of Wilson's Disease (WD): Case ReportZ S Gucev, N Pop-Jordanova, V Calovska, et al.The New England Journal of Medicine|January 8, 2015
TBX6 null variants and a common hypomorphic allele in congenital scoliosisN Wu, X Ming, J Xiao, et al.Pageof 2