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Human Heredity|September 28, 1998
DNA analysis of the fragile X syndrome in an at risk pediatric population in croatia: simple clinical preselection criteria can considerably improve the cost-effectiveness of fragile X screening studiesS Hećimović, I Barisić, K PavelićHuman Biology|April 4, 2009
Haplotype and AGG interspersion analysis of FMR1 alleles in a Croatian population: no founder effect detected in patients with fragile X syndromeH Dokić, I Barisić, V Culić, et al.Acta Paediatrica (Oslo, Norway : 1992)|July 13, 2002
Screening for fragile X syndrome: results from a school for mentally retarded childrenS Hećimović, I Petek Tarnik, I Barić, et al.Clinical Chemistry and Laboratory Medicine|January 19, 2002
A simple and rapid analysis of triplet repeat diseases by expand long PCRS Hećimović, J Vlasić, L Barisić, et al.Journal of Neurology|November 9, 2007
Oxidative stress parameters in plasma of Huntington's disease patients, asymptomatic Huntington's disease gene carriers and healthy subjects : a cross-sectional studyN Klepac, M Relja, R Klepac, et al.Clinical Genetics|October 23, 1997
Expand Long PCR for fragile X mutation detectionS Hećimović, I Barisić, A Müller, et al.Pageof 1