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Ece Solmaz, Asli
75
results:
Search for persons
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Format
Online (75)
Mediatypes
Articles (Online) (47)
OpenAccess-fulltext (28)
Languages
english (57)
Sorted by: Relevance
Sorted by: Year
?
1
A rare cause of primary amenorrhea: LHCGR gene mutations:
Aktar Karakaya, Amine
;
Çayır, Atilla
;
Unal, Edip
...
European Journal of Obstetrics & Gynecology and Reproductive Biology. 272 (2022) - p. 193-197 , 2022
Link:
https://doi.org/10.1016/..
?
2
A novel bi-allelic variant in the SDHB gene causes a severe..:
Ece Solmaz, Asli
;
Pariltay, Erhan
;
Talim, Beril
.
Clinical Neurology and Neurosurgery. 212 (2022) - p. 107039 , 2022
Link:
https://doi.org/10.1016/..
?
3
Mutation spectrum of the NF1 gene and genotype–phenotype co..:
Ece Solmaz, Asli
;
Isik, Esra
;
Atik, Tahir
..
Clinical Neurology and Neurosurgery. 208 (2021) - p. 106884 , 2021
Link:
https://doi.org/10.1016/..
?
4
Clinical Contribution of Next-Generation Sequencing Multige..:
Ece Solmaz, Aslı
;
Yeniay, Levent
;
Gökmen, Erhan
...
Clinical Breast Cancer. 21 (2021) 6 - p. e647-e653 , 2021
Link:
https://doi.org/10.1016/..
?
5
Targeted multi-gene panel testing for the diagnosis of Bard..:
Ece Solmaz, Asli
;
Onay, Huseyin
;
Atik, Tahir
...
European Journal of Medical Genetics. 58 (2015) 12 - p. 689-694 , 2015
Link:
https://doi.org/10.1016/..
?
6
Investigating the effects of PTEN mutations on cGAS-STING p..:
Dogan, Eda
;
Yildirim, Zafer
;
Akalin, Taner
...
Journal of Neuro-Oncology. 166 (2024) 2 - p. 283-292 , 2024
Link:
https://doi.org/10.1007/..
?
7
20-year experience on prenatal diagnosis in a reference uni..:
DURMAZ, Burak
;
BOLAT, Hilmi
;
CENGİSİZ, Zehra
...
TURKISH JOURNAL OF MEDICAL SCIENCES. 51 (2021) 4 - p. 1775-1780 , 2021
Link:
https://doi.org/10.3906/..
?
8
Clinical and molecular aspects of PTEN mutations in 10 pedi..:
Isik, Esra
;
Simsir, Ozguc Semih
;
Solmaz, Asli Ece
...
Annals of Human Genetics. 84 (2020) 4 - p. 324-330 , 2020
Link:
https://doi.org/10.1111/..
?
9
BRCA1-BRCA2 mutation analysis results in 910 individuals: M..:
Solmaz, Aslı Ece
;
Onay, Hüseyin
;
Yeniay, Levent
...
Cancer Genetics. 241 (2020) - p. 20-24 , 2020
Link:
https://doi.org/10.1016/..
?
10
The genetics of recurrent hydatidiform moles: new insights ..:
Nguyen, Ngoc Minh Phuong
;
Khawajkie, Yassemine
;
Mechtouf, Nawel
...
Modern Pathology. 31 (2018) 7 - p. 1116-1130 , 2018
Link:
https://doi.org/10.1038/..
?
11
Molecular spectrum of α-globin gene mutations in the Aegean..:
Onay, Hüseyin
;
Aykut, Ayça
;
Karaca, Emin
...
International Journal of Hematology. 102 (2015) 1 - p. 1-6 , 2015
Link:
https://doi.org/10.1007/..
?
12
Bardet Biedl sendromlu hastalarda moleküler analiz ile feno..:
Ece Solmaz, Aslı
Tez. , 2014
Link:
https://hdl.handle.net/1..
?
13
Bardet Biedl sendromlu hastalarda moleküler analiz ile feno..:
Ece Solmaz, Aslı
Tez. , 2014
Link:
https://hdl.handle.net/1..
?
14
Prevalence of lipoprotein lipase mutation in patients with ..:
Soyaltın, Utku Erdem
;
Hakverdi, Gülden
;
Şimşir, Ilgın Yıldırım
..
Ege Tıp Dergisi. , 2022
Link:
https://hdl.handle.net/1..
?
15
Prevalence of lipoprotein lipase mutation in patients with ..:
Hakverdi, Gülden
;
Soyaltın, Utku Erdem
;
Kandemir, Ayşe Bengü
..
Ege Tıp Dergisi. , 2022
Link:
https://hdl.handle.net/1..
1-15