Have a personal or library account? Click to login
Clinical next generation sequencing reveals an H3F3A gene as a new potential gene candidate for microcephaly associated with severe developmental delay, intellectual disability and growth retardation Cover

Clinical next generation sequencing reveals an H3F3A gene as a new potential gene candidate for microcephaly associated with severe developmental delay, intellectual disability and growth retardation

Balkan Journal of Medical Genetics
Volume 22 (2019): Issue 2 (November 2019)
By: A Maver,  G Čuturilo,  Stojanović J Ruml and  B Peterlin  
Open Access
|Dec 2019

Authors

A Maver

Clinical Institute of Genomic Medicine, University Medical Center Ljubljana, Ljubljana, Slovenia

G Čuturilo

Faculty of Medicine, University of Belgrade, Belgrade, Serbia
Department of Clinical Genetics, University Children’s Hospital, Belgrade, Serbia

Stojanović J Ruml

Department of Clinical Genetics, University Children’s Hospital, Belgrade, Serbia

B Peterlin

borut.peterlin@kclj.si

Clinical Institute of Genomic Medicine, University Medical Center Ljubljana, Ljubljana, Slovenia
DOI: https://doi.org/10.2478/bjmg-2019-0028 | Journal eISSN: 2199-5761
Journal RSS Feed
Language: English
Page range: 65 - 68
Published on: Dec 21, 2019
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Growth delay,
gene,
intellectual disability,
Microcephaly,
Severe developmental delay
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 2019 A Maver, G Čuturilo, Stojanović J Ruml, B Peterlin, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Previous articleVolume 22 (2019): Issue 2 (November 2019)Next article