Malan syndrome (Sotos syndrome 2) in two patients with 19p13.2 deletion encompassing NFIX gene and novel NFIX sequence variant.
- DOI
- 10.5507/bp.2016.006
- Published
- 2016 Mar
- Container
- Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.5507/bp.2016.006,
title = {Malan syndrome (Sotos syndrome 2) in two patients with 19p13.2 deletion encompassing NFIX gene and novel NFIX sequence variant.},
author = {Jezela-Stanek A and Kucharczyk M and Falana K and Jurkiewicz D and Mlynek M and Wicher D and Rydzanicz M and Kugaudo M and Cieslikowska A and Ciara E and Ploski R and Krajewska-Walasek M},
year = {2016},
journal = {Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia},
doi = {10.5507/bp.2016.006},
url = {https://doi.org/10.5507/bp.2016.006}
}RIS
TY - JOUR TI - Malan syndrome (Sotos syndrome 2) in two patients with 19p13.2 deletion encompassing NFIX gene and novel NFIX sequence variant. AU - Jezela-Stanek A AU - Kucharczyk M AU - Falana K AU - Jurkiewicz D AU - Mlynek M AU - Wicher D AU - Rydzanicz M AU - Kugaudo M AU - Cieslikowska A AU - Ciara E AU - Ploski R AU - Krajewska-Walasek M PY - 2016 JO - Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia DO - 10.5507/bp.2016.006 UR - https://doi.org/10.5507/bp.2016.006 ER -
APA
A, J., M, K., K, F., D, J., M, M., D, W., M, R., M, K., A, C., E, C., R, P., & M, K. (2016). Malan syndrome (Sotos syndrome 2) in two patients with 19p13.2 deletion encompassing NFIX gene and novel NFIX sequence variant.. Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia. https://doi.org/10.5507/bp.2016.006
Source records
- pubmed · retrieved 2026-09-26T16:22:47.092Z