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Global Medical Genetics|June 16, 2022
Psoriasis: An Immunogenetic PerspectiveAyca Kocaaga, Mustafa Kocaaga
Global Medical Genetics|June 16, 2022
Presentation of an Infant with Chromosome 18p Deletion Syndrome and Asymmetric Septal HypertrophyAyca Kocaaga, Sevgi Yimenicioglu
Revista Da Associacao Medica Brasileira (1992)|March 19, 2025
Investigation of the relationship between venous thromboembolism and thrombophilic variantsAyca Kocaaga, Müfide Okay Özgeyik
Molecular Biology Reports|December 3, 2022
Clinical, neuroimaging and genetic findings in children with hereditary ataxia: single center studyYasar Bildirici, Ayca Kocaaga, Sevgi Yimenicioglu
Indian Journal of Ophthalmology|July 6, 2022
Novel <i>NR2F1</i> variant identified by whole-exome sequencing in a patient with Bosch-Boonstra-Schaaf optic atrophy syndromeAyca Kocaaga, Sevgi Yimenicioglu, Haluk Hüseyin Gürsoy
Annals of Saudi Medicine|November 29, 2022
The pattern of chromosomal abnormalities in recurrent miscarriages: a single center retrospective studyAyca Kocaaga, Halime Kilic, Sevgi Gulec
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|February 16, 2026
Multigene panel testing reveals the spectrum of non-BRCA germline variants in BRCA1/2-negative breast, ovarian, and prostate cancer patients from a Turkish cohortBarıs Paksoy, Ozgur Erkal, Ayca Kocaaga
Revista Da Associacao Medica Brasileira (1992)|November 1, 2023
The genetic spectrum of polycystic kidney disease in childrenAyca Kocaaga, Yesim Özdemir Atikel, Mehtap Sak, et al.
Pediatrics and Neonatology|August 24, 2022
Diagnosis and genetic analysis of polycythemia in children and a novel EPAS1 gene mutationHatice Mine Cakmak, Omer Kartal, Ayca Kocaaga, et al.
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