De novo KMT2D heterozygous frameshift deletion in a newborn with a congenital heart anomaly
, , oraz
26 sie 2020
O artykule
Kategoria artykułu: Case Report
Data publikacji: 26 sie 2020
Zakres stron: 83 - 90
DOI: https://doi.org/10.2478/bjmg-2020-0008
Słowa kluczowe
© 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