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Rare case of a heterozygous microdeletion 9q21.11-q21.2: Clinical and genetic characteristics Cover

Rare case of a heterozygous microdeletion 9q21.11-q21.2: Clinical and genetic characteristics

Open Access
|Dec 2018

Authors

HY Ivanov

doctorhristoivanov@yahoo.com

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
Language: English
Page range: 59 - 62
Published on: Dec 31, 2018
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year

© 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.