A Little Known but Very Common Phenotype in Patients With Severe Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Insufficiency.
- DOI
- 10.1002/pbc.31591
- Published
- 2025 May
- Container
- Pediatric blood & cancer
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/pbc.31591,
title = {A Little Known but Very Common Phenotype in Patients With Severe Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Insufficiency.},
author = {Kızılay DÖ and Karapınar DY and Karadaş N and Karaoğlan M and Akbayram S and Gökşen D and Gadashova A and Albayrak S and Şahinoğlu EP and Orbak Z and Bıçakçı Z and Akın L and Albayrak C and Koç C and Ünüvar A and Anık A and Aral YZ and Cimbek EA and Bahadır A and Mete C and Özen S},
year = {2025},
journal = {Pediatric blood \& cancer},
doi = {10.1002/pbc.31591},
url = {https://doi.org/10.1002/pbc.31591}
}RIS
TY - JOUR TI - A Little Known but Very Common Phenotype in Patients With Severe Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Insufficiency. AU - Kızılay DÖ AU - Karapınar DY AU - Karadaş N AU - Karaoğlan M AU - Akbayram S AU - Gökşen D AU - Gadashova A AU - Albayrak S AU - Şahinoğlu EP AU - Orbak Z AU - Bıçakçı Z AU - Akın L AU - Albayrak C AU - Koç C AU - Ünüvar A AU - Anık A AU - Aral YZ AU - Cimbek EA AU - Bahadır A AU - Mete C AU - Özen S PY - 2025 JO - Pediatric blood & cancer DO - 10.1002/pbc.31591 UR - https://doi.org/10.1002/pbc.31591 ER -
APA
DÖ, K., DY, K., N, K., M, K., S, A., D, G., A, G., S, A., EP, Ş., Z, O., Z, B., L, A., C, A., C, K., A, Ü., A, A., YZ, A., EA, C., A, B., C, M., & S, Ö. (2025). A Little Known but Very Common Phenotype in Patients With Severe Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Insufficiency.. Pediatric blood & cancer. https://doi.org/10.1002/pbc.31591
Source records
- pubmed · retrieved 2026-11-10T07:08:20.738Z