Rare case of a heterozygous microdeletion 9q21.11-q21.2: Clinical and genetic characteristics
By: HY Ivanov, V Stoyanova, I Ivanov, A Linev, R Vazharova, S Ivanov, L Balabanski and D Toncheva
Authors
HY Ivanov
Department of Pediatrics and Medical Genetics, Medical University Plovdiv, Plovdiv, Bulgaria
V Stoyanova
Department of Pediatrics and Medical Genetics, Medical University Plovdiv, Plovdiv, Bulgaria
Department of Medical Genetics, University Hospital “St. George,”, Plovdiv, Bulgaria
I Ivanov
Department of Pediatrics and Medical Genetics, Medical University Plovdiv, Plovdiv, Bulgaria
Department of Medical Genetics, University Hospital “St. George,”, Plovdiv, Bulgaria
A Linev
Department of Pediatrics and Medical Genetics, Medical University Plovdiv, Plovdiv, Bulgaria
Department of Medical Genetics, University Hospital “St. George,”, Plovdiv, Bulgaria
R Vazharova
Department of Biology, Medical Genetics and Microbiology, Sofia University “St. Kliment Ohridski,”, Sofia, Bulgaria
Department of Genomics, Hospital “Dr. Malinov,”, Sofia, Bulgaria
S Ivanov
Department of Genomics, Hospital “Dr. Malinov,”, Sofia, Bulgaria
L Balabanski
Department of Genomics, Hospital “Dr. Malinov,”, Sofia, Bulgaria
D Toncheva
Department of Genomics, Hospital “Dr. Malinov,”, Sofia, Bulgaria
Department of Medical Genetics, Medical University Sofia, Sofia, Bulgaria
DOI: https://doi.org/10.2478/bjmg-2018-0021 | Journal eISSN: 2199-5761
Language: English
Page range: 59 - 62
Published on: Dec 31, 2018
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
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© 2018 HY Ivanov, V Stoyanova, I Ivanov, A Linev, R Vazharova, S Ivanov, L Balabanski, D Toncheva, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.