De novo KMT2D heterozygous frameshift deletion in a newborn with a congenital heart anomaly
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Aug 26, 2020
About this article
Article Category: Case Report
Published Online: Aug 26, 2020
Page range: 83 - 90
DOI: https://doi.org/10.2478/bjmg-2020-0008
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© 2020 Stangler Herodež Š, Marčun Varda N, Kokalj Vokač N, Krgović D, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Stangler Herodež, Š
Laboratory of Medical Genetics, University Medical Centre MariborMaribor, Slovenia
Medical Faculty, University of MariborMaribor, Slovenia
Marčun Varda, N
Medical Faculty, University of MariborMaribor, Slovenia
Division of Paediatrics, University Medical Centre MariborMaribor, Slovenia
N, Kokalj Vokač
Laboratory of Medical Genetics, University Medical Centre MariborMaribor, Slovenia
Medical Faculty, University of MariborMaribor, Slovenia
Krgović, D
Laboratory of Medical Genetics, University Medical Centre MariborMaribor, Slovenia
Medical Faculty, University of MariborMaribor, Slovenia