A rare case of patient with neurofibromatosis type 1 in a genotype-phenotype correlation revealing a submicroscopic deletion on the long arm of chromosome 17.
- DOI
- 10.1002/ccr3.4047
- Published
- 2021 Apr
- Container
- Clinical case reports
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1002/ccr3.4047,
title = {A rare case of patient with neurofibromatosis type 1 in a genotype-phenotype correlation revealing a submicroscopic deletion on the long arm of chromosome 17.},
author = {Yethindra V and Tagaev T and Mamytova E and Mainazarova E and Dzhumakova C and Namazbekova A},
year = {2021},
journal = {Clinical case reports},
doi = {10.1002/ccr3.4047},
url = {https://doi.org/10.1002/ccr3.4047}
}RIS
TY - JOUR TI - A rare case of patient with neurofibromatosis type 1 in a genotype-phenotype correlation revealing a submicroscopic deletion on the long arm of chromosome 17. AU - Yethindra V AU - Tagaev T AU - Mamytova E AU - Mainazarova E AU - Dzhumakova C AU - Namazbekova A PY - 2021 JO - Clinical case reports DO - 10.1002/ccr3.4047 UR - https://doi.org/10.1002/ccr3.4047 ER -
APA
V, Y., T, T., E, M., E, M., C, D., & A, N. (2021). A rare case of patient with neurofibromatosis type 1 in a genotype-phenotype correlation revealing a submicroscopic deletion on the long arm of chromosome 17.. Clinical case reports. https://doi.org/10.1002/ccr3.4047
Source records
- pubmed · retrieved 2026-09-26T18:48:36.419Z