M. Hasanhodžić

Management goals for type 1 Gaucher disease: An expert consensus document from the European working group on Gaucher disease.

D. Zafeiriou, P. Iversen, J. Szer, 2018, Blood cells, molecules & diseases.

Neonatal bacterial meningitis: Results from a cross-sectional hospital based study.

H. Tahirovič, Izeta Softić, M. Hasanhodžić, 2015, Acta medica academica.

Diagnostics of common microdeletion syndromes using fluorescence in situ hybridization: Single center experience in a developing country

A. Kurtovic-Kozaric, S. Dinarevic, F. Catibusic, 2016, Bosnian journal of basic medical sciences.

Clinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndrome

K. Koehler, A. Huebner, H. Tahirovič, 2009, European Journal of Pediatrics.

Down Syndrome and thyroid gland.

H. Tahirovič, L. Lukinac, M. Hasanhodžić, 2006, Bosnian journal of basic medical sciences.

Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss

B. Peterlin, A. Maver, N. Teran, 2018, PloS one.

FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature

K. Girisha, A. Shukla, B. Loeys, 2018, BMC Medical Genetics.