Vol. 57 No. 4 (2013)

Published: 2013-12-30

Review

  • Next generation sequencing – towards translation into clinical practice

    Aleš Maver, Borut Peterlin
    295-300
    DOI: https://doi.org/10.13112/pc.650
  • Forensic DNA application: an interdisciplinary perspective

    Petar Projić, Gordan Lauc, Dragan Primorac
    301-311
    DOI: https://doi.org/10.13112/pc.651
  • Epigenetics in reproduction and development

    Floriana Bulić-Jakuš
    312-317
    DOI: https://doi.org/10.13112/pc.652
  • Pharmacogenetics in clinical practice – Recommendations and guidelines

    Nada Božina, Lana Pejnović
    318-330
    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
    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
    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
    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
    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
    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
    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
    DOI: https://doi.org/10.13112/pc.661
  • Chorionic villus sampling

    Ana Vičić, Feodora Stipoljev
    374-381
    DOI: https://doi.org/10.13112/pc.662
  • New microdeletion syndromes

    Ingeborg Barišić, Leona Morožin Pohovski
    382-389
    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
    DOI: https://doi.org/10.13112/pc.664