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Anlas, Özlem
17
results:
Search for persons
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Online (17)
Mediatypes
Articles (Online) (7)
OpenAccess-fulltext (10)
Languages
english (15)
Sorted by: Relevance
Sorted by: Year
?
1
Detection of 13 Novel Variants and Investigation of Mutatio..:
Ozalp, Ozge
;
Anlas, Ozlem
Indian Journal of Hematology and Blood Transfusion. 40 (2023) 2 - p. 268-280 , 2023
Link:
https://doi.org/10.1007/..
?
2
A Rare Cause of Paroxysmal Movement Disorder Associated wit..:
Sarıgecılı, Esra
;
Anlas, Ozlem
Annals of Indian Academy of Neurology. 26 (2023) 3 - p. 290-293 , 2023
Link:
https://doi.org/10.4103/..
?
3
HLA DQ2 and HLA DQ8 genetic evaluation in children with Typ..:
Ata, Aysun
;
Anlaş, Özlem
;
Gülcü Taşkın, Didem
Medical Science and Discovery. 10 (2023) 3 - p. 178-181 , 2023
Link:
https://doi.org/10.36472..
?
4
An unusual manifestation in a pediatric patient with MAFB m..:
Kisla Ekinci, Rabia Miray
;
Ozalp, Ozge
;
Anlas, Ozlem
...
International Journal of Rheumatic Diseases. 26 (2023) 10 - p. 2064-2068 , 2023
Link:
https://doi.org/10.1111/..
?
5
Utility of a targeted next-generation sequencing-based gene..:
Miray Kışla Ekinci, Rabia
;
Anlaş, Özlem
;
Özalp, Özge
Archives of Rheumatology. 38 (2022) 2 - p. 299-306 , 2022
Link:
https://doi.org/10.46497..
?
6
A rare cause of microcephaly, thin corpus callosum and refr..:
Sarigecili, Esra
;
Bulut, Fatma Derya
;
Anlas, Ozlem
Clinical Neurology and Neurosurgery. 218 (2022) - p. 107283 , 2022
Link:
https://doi.org/10.1016/..
?
7
Clinical presentation of children with Deficiency of Adenos..:
Kisla Ekinci, Rabia Miray
;
Anlas, Ozlem
;
Ozalp, Ozge
European Journal of Medical Genetics. 65 (2022) 8 - p. 104555 , 2022
Link:
https://doi.org/10.1016/..
?
8
Dicentric Recombinant Chromosome 18 due to Maternal Paracen..:
Bağcı, Gülseren
;
Gunduz, Cavidan Nur Semerci
;
Anlas, Özlem
...
Molecular Syndromology. , 2023
Link:
https://hdl.handle.net/1..
?
9
A Rare Cause of Paroxysmal Movement Disorder Associated wit..:
Sarıgecılı, Esra
;
Anlas, Ozlem
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10394464/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
10
Utility of a targeted next-generation sequencing-based gene..:
Kışla Ekinci, Rabia Miray
;
Anlaş, Özlem
;
Özalp, Özge
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10481688/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
11
A case of recombinant chromosome 4: further delineation of ..:
Düzcan, Füsun
;
Anlaş, Özlem
;
Çetin, G. Ozan
...
Pamukkale Tıp Dergisi. , 2020
Link:
https://hdl.handle.net/1..
?
12
A case of recombinant chromosome 4: Further delineation of ..:
Anlaş, Özlem
;
Çetin, Gökhan Ozan
;
Yararbaş, Kanay
...
Pamukkale Medical Journal. , 2020
Link:
https://hdl.handle.net/2..
?
13
A Novel Nonsense Mutation In The EYA1 Gene Found In A Patie..:
Albuz, Burcu
;
Zeybek, Selcan
;
Anlas, Özlem
...
EUROPEAN JOURNAL OF HUMAN GENETICS. , 2019
Link:
https://hdl.handle.net/1..
?
14
The co-existence of Nablus Mask-Like Facial Syndrome and Kl..:
Anlaş, Özlem
;
Sarikepe, B
;
Zeybek, Selcan
...
EUROPEAN JOURNAL OF HUMAN GENETICS. , 2019
Link:
https://hdl.handle.net/1..
?
15
Erken başlangıçlı ve idiyopatik parkinson hastalarında GBA ..:
Anlaş, Özlem
Tez. , 2017
Link:
https://hdl.handle.net/1..
1-15