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I Barisić

Showing results (1-10 of 18) with videos related to

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Jugoslavenska Ginekologija I Perinatologija|January 1, 1987
[The attitude of women to the use of early amniocentesis and chorionic villi technics--psychologic aspects]L Zergollern, I Barisić
Acta Medica Iugoslavica|January 1, 1985
[Chromosome abnormalities in couples with habitual spontaneous abortions]L Zergollern, I Barisić
Lijecnicki Vjesnik|April 1, 1987
[Ring chromosome 13 (case report)]L Zergollern, I Barisić
Acta Medica Iugoslavica|January 1, 1988
[Heterogeneity in osteogenesis imperfecta]L Zergollern, I Barisić, S Zergollern
Journal of Medical Genetics|October 1, 1996
Megalocornea-mental retardation syndrome: report of a new caseI Barisić, I Ligutić, L Zergollern
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 Pavelić
Lijecnicki Vjesnik|January 1, 1996
[Mucolipidosis type III (case report)]I Ligutić, I Barisić, K Fumić, et al.
Clinical Genetics|March 1, 1996
Risk estimates for balanced reciprocal translocation carriers--prenatal diagnosis experienceI Barisić, L Zergollern, D Muzinić, et al.
Clinical Genetics|December 1, 1996
Unusual segregation of t(11;22) resulting from crossing-over followed by 3:1 disjunction at meiosis II Petković, A de Capoa, P Giancotti, et al.
Human 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.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Jugoslavenska Ginekologija I Perinatologija|January 1, 1987
[The attitude of women to the use of early amniocentesis and chorionic villi technics--psychologic aspects]L Zergollern, I Barisić
Acta Medica Iugoslavica|January 1, 1985
[Chromosome abnormalities in couples with habitual spontaneous abortions]L Zergollern, I Barisić
Lijecnicki Vjesnik|April 1, 1987
[Ring chromosome 13 (case report)]L Zergollern, I Barisić
Acta Medica Iugoslavica|January 1, 1988
[Heterogeneity in osteogenesis imperfecta]L Zergollern, I Barisić, S Zergollern
Journal of Medical Genetics|October 1, 1996
Megalocornea-mental retardation syndrome: report of a new caseI Barisić, I Ligutić, L Zergollern
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 Pavelić
Lijecnicki Vjesnik|January 1, 1996
[Mucolipidosis type III (case report)]I Ligutić, I Barisić, K Fumić, et al.
Clinical Genetics|March 1, 1996
Risk estimates for balanced reciprocal translocation carriers--prenatal diagnosis experienceI Barisić, L Zergollern, D Muzinić, et al.
Clinical Genetics|December 1, 1996
Unusual segregation of t(11;22) resulting from crossing-over followed by 3:1 disjunction at meiosis II Petković, A de Capoa, P Giancotti, et al.
Human 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.
Pageof 2