Metrikler
Yayın
9
Açık Erişim
2
Makaleler
Tümü (8)
SCI-E, SSCI, AHCI (5)
SCI-E, SSCI, AHCI, ESCI (8)
ESCI (3)
Scopus (7)
TRDizin (1)
2021
20211. The Association of MCP-1 Level and MCP-1 -2518 A/G and CCR2 190 G/A Gene Polymorphisms with COPD and Pulmonary Hypertension
YILDIRIM M. E., BERK S., KÜÇÜK KURTULGAN H., TEKİN G., TEKİN Y. K., BAŞER B., et al.
GAZI MEDICAL JOURNAL
, cilt.32, sa.1, ss.28-32, 2021 (ESCI, Scopus)
2020
20202. Analysis of PKD1 and PKD2 Gene Mutations for Autosomal Dominant Polycystic Kidney Disease Cases in Turkish Population
SEZGİN İ., KAYATAŞ M., KÜÇÜK KURTULGAN H., YILDIRIM M. E., BAŞER B., TİMÜÇİN M., et al.
TURKISH JOURNAL OF NEPHROLOGY
, cilt.29, sa.4, ss.304-309, 2020 (ESCI)
2019
20193. Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia
YILDIRIM M. E., Kurtulgan H. K., ÖZDEMİR Ö., KILIÇGÜN H., Aydemir D. S., Baser B., et al.
ANNALS OF SAUDI MEDICINE
, cilt.39, sa.6, ss.382-387, 2019 (SCI-Expanded, Scopus)
2019
20194. The type and prevalence of chromosomal abnormalities in couples with recurrent first trimester abortions: A Turkish retrospective study
YILDIRIM M. E., KARAKUŞ S., Kurtulgan H. K., Baser B., Sezgin I.
JOURNAL OF GYNECOLOGY OBSTETRICS AND HUMAN REPRODUCTION
, cilt.48, sa.7, ss.521-525, 2019 (SCI-Expanded, Scopus)
2019
20195. Ocular and Genetic Characteristics Observed in Two Cases of Fish-Eye Disease
Ustaoglu M., Solmaz N., BAŞER B., KÜÇÜK KURTULGAN H., Onder F.
CORNEA
, cilt.38, sa.3, ss.379-383, 2019 (SCI-Expanded)
2018
20186. A case of weill-marchesani syndrome with a novel mutation and vitamin d deficiency
YILDIRIM M. E., VURAL ÖZEÇ A., KÜÇÜK KURTULGAN H., KILIÇGÜN H., BAŞER B.
JOURNAL OF CLINICAL AND ANALYTICAL MEDICINE
, cilt.9, sa.6, ss.578-580, 2018 (ESCI)
2018
20187. Megacystis Microcolon Intestinal Hypoperistalsis Syndrome in Which a Different De Novo Actg2 Mutation was Detected: A Case Report
Korgali E., YAVUZ A., ÇAĞLAR ŞİMŞEK C. E., GÜNEY C., KÜÇÜK KURTULGAN H., BAŞER B., et al.
FETAL AND PEDIATRIC PATHOLOGY
, cilt.37, sa.2, ss.109-116, 2018 (SCI-Expanded, Scopus)
2017
20178. 8q22.3 q24.23 duplication in a patient with oral frenulum and normal intellectual development
KÜÇÜK KURTULGAN H., YILDIRIM M. E., BAŞER B., SEZGİN İ.
MOLECULAR CYTOGENETICS
, cilt.10, 2017 (SCI-Expanded)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler
2017
20171. 8q22.3 q24.23 duplication in a patient with oral frenulum andnormal intellectual development
KÜÇÜK KURTULGAN H., YILDIRIM M. E., BAŞER B., SEZGİN İ.
11th European Cytogenetics Conference, İtalya, 1 - 04 Temmuz 2017, cilt.10, ss.19, (Özet Bildiri)