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Balkan Journal of Medical Genetics
Volume 22 (2019): Issue 2 (November 2019)
Open Access
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
A Maver
A Maver
,
G Čuturilo
G Čuturilo
,
Stojanović J Ruml
Stojanović J Ruml
and
B Peterlin
B Peterlin
| Dec 21, 2019
Balkan Journal of Medical Genetics
Volume 22 (2019): Issue 2 (November 2019)
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Article Category:
Case Report
Published Online:
Dec 21, 2019
Page range:
65 - 68
DOI:
https://doi.org/10.2478/bjmg-2019-0028
Keywords
Growth delay
,
gene
,
intellectual disability
,
Microcephaly
,
Severe developmental delay
© 2019 Maver A, Čuturilo G, Ruml Stojanović J, Peterlin B, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.