A Little Known but Very Common Phenotype in Patients With Severe Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Insufficiency
Makaleler > Tam Makale · 2025
Yazarlar: Deniz ÖZALP KIZILAY, Deniz YILMAZ KARAPINAR, Nihal KARADAŞ, MURAT KARAOĞLAN, SİNAN AKBAYRAM, Ruhsar Damla GÖKŞEN, Ayşe Gadaşova, SERPİL ALBAYRAK, ESRA PEKPAK ŞAHİNOĞLU, ZERRİN ORBAK, ZAFER BIÇAKÇI, LEYLA AKIN, CANAN ALBAYRAK, CANSU KOÇ, AYŞEGÜL ÜNÜVAR, AHMET ANIK, YUSUF ZİYA ARAL, EMİNE AYÇA CİMBEK, AYŞENUR BAHADIR, CEM METE, Samim ÖZEN
PEDIATRIC BLOOD & CANCER, SCI Expanded İndekslerine Giren Dergi, Uluslararası, 2025, cilt 72, ss 10-16
DOI: 10.1002/pbc.31591