Benign, pathogenic and copy number variations of unknown clinical significance in patients with congenital malformations and developmental delay
By: M Mihaylova, R Staneva, D Toncheva, M Pancheva and S Hadjidekova
Authors
M Mihaylova
Department of Medical Genetics, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria
R Staneva
Department of Medical Genetics, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria
Woman Health Hospital “Nadezhda”, Sofia, Bulgaria
D Toncheva
Department of Medical Genetics, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria
M Pancheva
Department of Medical Genetics, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria
Woman Health Hospital “Nadezhda”, Sofia, Bulgaria
S Hadjidekova
Department of Medical Genetics, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria
Woman Health Hospital “Nadezhda”, Sofia, Bulgaria
Language: English
Page range: 5 - 12
Published on: Jun 30, 2017
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Related subjects:
© 2017 M Mihaylova, R Staneva, D Toncheva, M Pancheva, S Hadjidekova, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.