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
By: A Maver, G Čuturilo, Stojanović J Ruml and B Peterlin
DOI: https://doi.org/10.2478/bjmg-2019-0028 | Journal eISSN: 2199-5761
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
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© 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.