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Atik, Tahir
193
results:
Search for persons
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Format
Online (193)
Mediatypes
Articles (Online) (52)
OpenAccess-fulltext (141)
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english (163)
Sorted by: Relevance
Sorted by: Year
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1
Further defining the molecular spectrum and long‐term follo..:
Akalın, Akçahan
;
Ayaz, Ercan
;
Soğukpınar, Merve
...
American Journal of Medical Genetics Part A. , 2024
Link:
https://doi.org/10.1002/..
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2
The Utility of Genetic Testing in Infantile Epileptic Spasm..:
Kanmaz, Seda
;
Yılmaz, Sanem
;
Olculu, Cemile Büşra
...
Pediatric Neurology. 157 (2024) - p. 100-107 , 2024
Link:
https://doi.org/10.1016/..
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3
Genetic heterogeneity in hereditary hearing loss: Potential..:
Ramzan, Memoona
;
Zafeer, Mohammad Faraz
;
Abad, Clemer
...
European Journal of Human Genetics. 32 (2024) 6 - p. 639-646 , 2024
Link:
https://doi.org/10.1038/..
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4
O-09 A rare cause of acute pancreatitis: Werner Syndrome:
Şakar, Kenan
;
Akıncı, Barış
;
Yıldırım Şimşir, Ilgın
...
JCEM Case Reports. 2 (2024) Supplement_1 - p. , 2024
Link:
https://doi.org/10.1210/..
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5
Genome sequencing identifies coding and non-coding variants..:
Ramzan, Memoona
;
Duman, Duygu
;
Hendricks, LeShon Chere Peart
...
Journal of Human Genetics. 68 (2023) 10 - p. 657-669 , 2023
Link:
https://doi.org/10.1038/..
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6
Molecular diagnosis in patients with monogenic diabetes mel..:
Goksen, Damla
;
Evin, Ferda
;
Isik, Esra
...
Diabetes Research and Clinical Practice. 205 (2023) - p. 110953 , 2023
Link:
https://doi.org/10.1016/..
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7
Association between vitamin D receptor gene FokI polymorphi..:
Bozgul, Sukriye Miray Kilincer
;
Emecen, Durdugul Ayyildiz
;
Akarca, Funda Karbek
...
Molecular Biology Reports. 51 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1007/..
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8
Pelvis Magnetic Resonance Imaging to Diagnose Familial Part..:
Adiyaman, Suleyman Cem
;
Altay, Canan
;
Kamisli, Berfu Y
...
The Journal of Clinical Endocrinology & Metabolism. 108 (2023) 8 - p. e512-e520 , 2023
Link:
https://doi.org/10.1210/..
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9
Clinical features of generalized lipodystrophy in Turkey: A..:
Yildirim Simsir, Ilgin
;
Tuysuz, Beyhan
;
Ozbek, Mehmet Nuri
...
Diabetes, Obesity and Metabolism. 25 (2023) 7 - p. 1950-1963 , 2023
Link:
https://doi.org/10.1111/..
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10
Evaluation of social cognition, autistic traits, and dysmor..:
Ozbaran, Nazli Burcu
;
Ozyasar, Senay Celenay
;
Dogan, Nurhak
...
Clinical Child Psychology and Psychiatry. 27 (2022) 4 - p. 991-1005 , 2022
Link:
https://doi.org/10.1177/..
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11
LSM1 is the new candidate gene for neurodevelopmental disor..:
Kok Kilic, Gizem
;
Isik, Esra
;
Alpay, Omer
...
European Journal of Medical Genetics. 65 (2022) 11 - p. 104610 , 2022
Link:
https://doi.org/10.1016/..
?
12
C20orf24: A potential novel gene responsible for Cerebrofac..:
Isik, Esra
;
Emecen, Durdugul Ayyildiz
;
Atik, Tahir
..
European Journal of Medical Genetics. 65 (2022) 11 - p. 104621 , 2022
Link:
https://doi.org/10.1016/..
?
13
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/..
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14
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/..
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15
SURF1 related Leigh syndrome: Clinical and molecular findin..:
Kose, Melis
;
Canda, Ebru
;
Kagnici, Mehtap
...
Molecular Genetics and Metabolism Reports. 25 (2020) - p. 100657 , 2020
Link:
https://doi.org/10.1016/..
1-15