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Vol. 57 No. 4 (2013)
Vol. 57 No. 4 (2013)
Published:
2013-12-30
Review
Next generation sequencing – towards translation into clinical practice
Aleš Maver, Borut Peterlin
295-300
PDF
DOI:
https://doi.org/10.13112/pc.650
Forensic DNA application: an interdisciplinary perspective
Petar Projić, Gordan Lauc, Dragan Primorac
301-311
PDF
DOI:
https://doi.org/10.13112/pc.651
Epigenetics in reproduction and development
Floriana Bulić-Jakuš
312-317
PDF
DOI:
https://doi.org/10.13112/pc.652
Pharmacogenetics in clinical practice – Recommendations and guidelines
Nada Božina, Lana Pejnović
318-330
PDF
DOI:
https://doi.org/10.13112/pc.653
Genetics in the understanding of the hypoplastic left heart syndrome
Ivan Malčić, Andrea Dasović-Buljević, Josipa Grgat
331-337
PDF
DOI:
https://doi.org/10.13112/pc.654
Spinal muscular atrophy – molecular genetics in diagnosis and therapy
Nina Barišić, Vanja Ivanović, Ivan Lehman, Petra Grđan
338-343
PDF
DOI:
https://doi.org/10.13112/pc.655
Mucopolysaccharides: challenges on the path to treatment
Ksenija Fumić, Karmen Bilić, Marija Zekušić, Ana Škaričić, Ivo Barić
344-349
PDF
DOI:
https://doi.org/10.13112/pc.656
Newborn screening in Croatia and around the world
Danijela Petković Ramadža, Vladimir Sarnavka, Ana Škaričić, Ksenija Fumić, Ivo Barić
350-357
PDF
DOI:
https://doi.org/10.13112/pc.657
The importance of epidemiological studies for genetic concepts: examples from pediatric cardiology
Ivan Malčić, Daniel Dilber, Nataša Rojnić Putarek
358-364
PDF
DOI:
https://doi.org/10.13112/pc.658
Cytogenetic European Quality Assessment
Bojana Brajenović-Milić, Jadranka Vraneković, Ivana Babić Božović, Alena Buretić-Tomljanović
365-368
PDF
DOI:
https://doi.org/10.13112/pc.659
The International System for Human Cytogenetic Nomenclature – ISCN 2013: new issue changes and amendments
Leona Morožin Pohovski
369-373
PDF
DOI:
https://doi.org/10.13112/pc.661
Chorionic villus sampling
Ana Vičić, Feodora Stipoljev
374-381
PDF
DOI:
https://doi.org/10.13112/pc.662
New microdeletion syndromes
Ingeborg Barišić, Leona Morožin Pohovski
382-389
PDF
DOI:
https://doi.org/10.13112/pc.663
Molecular analysis of the MECP2 gene in female patients with Rett syndrome
Ivona Sansović, Katja Dumić Kubat, Ingeborg Barišić
390-397
PDF
DOI:
https://doi.org/10.13112/pc.664
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