Figure 1
Figure 2
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.](https://sciendo-parsed.s3.eu-central-1.amazonaws.com/647107e72b88470fbea144d8/j_bjmg-2018-0021_fig_003.jpg?X-Amz-Algorithm=AWS4-HMAC-SHA256&X-Amz-Content-Sha256=UNSIGNED-PAYLOAD&X-Amz-Credential=ASIA6AP2G7AKMD24L443%2F20260311%2Feu-central-1%2Fs3%2Faws4_request&X-Amz-Date=20260311T072306Z&X-Amz-Expires=3600&X-Amz-Security-Token=IQoJb3JpZ2luX2VjEI7%2F%2F%2F%2F%2F%2F%2F%2F%2F%2FwEaDGV1LWNlbnRyYWwtMSJHMEUCIQCb2HjEqKqD%2FjjUNxljDlPZfil7WL7qOhVUJdZJ07t5NgIgIeSlQmhNjXjsZTt5OZiLKVPK%2BcKN8ONZmS2DW5BBxvQqvAUIVxACGgw5NjMxMzQyODk5NDAiDPwYkQawSYFx9F2FGSqZBYjA3wIRYOSdGtvKVo8A7irtJnEw0xFsl6ToUNTzxvemJb6VfYJIvRcstt5GQEuH4BVxpKH3QYqEJ4c%2FAi2ese2Cm17gkTULxMQdX8cNIYK4jRuUZTa1%2FV9IQren6A4sdGrpeRh7UHa8Obxs59NHUoNfG7NCSLCjyUo6tPCaFy0Jn9qnVvPj7xRwepF00X7VC%2F5dD6XnBfXEfUbFPcCtwVD5fMSdlwRK%2FY4sjUeheP7xQ4yzLMHtAWqsVMIYQ6UmKjtKZrxAPhNCV8mRZAVwXdif7BCUAY1AisOzcljj99u2HHM6ZnS%2Fg7Iji5nfWVt6xWPAacyFuwcFxwq8s99vLAKhPAim%2BhCGuRIKuApJme9QOm6s4oA9AgLqfQw4C%2F1lGZ1KuVMFJTAshNzqOUoy%2FyTVwE7cgvaIGavRS%2FvUeSQekzL7vbLxQcPoKhTmGEK5Pk%2Fkxxz2Ydsz%2F4pTeWJsIlH%2Bmq0OtXIO6zYuwBR3pcdeVak%2BYVvgxVqggpcc6t04FBuz34bzuREIH%2B0tNL8bCxKUjAZgjIP2%2BPk2ssHd62QtdH6KMbfqHziP9yn92F7mmz7izggFFw02D3CSrmuQeXr4a9TM1rSwL5VW%2FH1XpxfwrEXFKmWADGtvDAh%2BpVcyCZwwsDOvhAaNfn%2BjR%2BONN9cov7hIgpsg%2BZ4GnrFWrKKvHTsLKNroXrYKsVnbDTioE1amjSsa6bC1j0oS%2F%2BU924UDYj8GPQ2CJISMdnw52%2Bxgx%2BB8OCcHan1xhEIs1BnBDgmPFqT%2B2H2rhH7CPhX%2FUe9MW2OsRDCWqGj%2FFFwW3SDryt%2FPRYLembcN%2FDr48LtEHESZs5ujVIjkPkDm4FHen%2BMS5ktwAMyTGqS8gVAqNQU2UXOvF8k66Cy8MJCBxM0GOrEBB7dxOBcRA7CJGUQ5qqJSoEdi1%2BrNeK5K2i3fgsnpCGF4LO2EHV7Tw%2FZLCbhTMv%2FWS7N6%2BrpA7n4D4HUVt7x7NroNFkmBX1vv1EBBuCOELc70I462I9pI%2FrJlApFuYLE%2BQyR22k8x25zHt04QpnSDHm5JlvBTbB9ZFqjk%2FAAaseaJZLULizX7lpajRe%2FmjgZw7xP7vGkHhzwS7hDOcHWsBLkgBKFUcmV7RRD14plkC5gn&X-Amz-Signature=bdc2e2e4bba6badd9b00a78684321ec9954603468114eeb11a1a90956db19c8e&X-Amz-SignedHeaders=host&x-amz-checksum-mode=ENABLED&x-id=GetObject)
Figures & Tables
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
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
Related subjects:
© 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.