Makaleler
Tümü (2)
SCI-E, SSCI, AHCI (2)
SCI-E, SSCI, AHCI, ESCI (2)
Scopus (2)
2022
20221. A Novel Intronic Mutation Reduces HAX1 Level and is Associated With Severe Congenital Neutropenia
GÖKTAŞ S., Azizoglu Z. B., Petersheim D., ERDOĞAN M., Eke Gungor H., Bisgin A., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.44, sa.1, 2022 (SCI-Expanded, Scopus)
2011
20112. PARTIAL TRISOMY 3q IN A CHILD WITH SACROCOCCYGEAL TERATOMA AND CORNELIA DE LANGE SYNDROME PHENOTYPE
Dundar M., Uzak A., ERDOĞAN M., SAATÇİ Ç., AKDENİZ Ş., Luleci G., et al.
GENETIC COUNSELING
, cilt.22, sa.2, ss.199-205, 2011 (SCI-Expanded, Scopus)