Figure 1
Phenotype of the proband.
Figure 2
Karyotype of the proband.
Figure 3
Graphical representation of chromosome 9 of the patient is shown. The deleted region of 9q is marked in red: arr [hg19] 9q21.11q21.2 (71034203-80689990) x1.
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
DOI: https://doi.org/10.2478/bjmg-2018-0021 | Journal eISSN: 2199-5761 (formerly 1311-0160) | Journal ISSN: 1311-0160
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
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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.