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Anlaş, Özlem
17  Ergebnisse:
Personensuche X
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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/..
 
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2

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/..
 
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3

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/..
 
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4

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..
 
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5

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/..
 
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6

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..
 
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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/..
 
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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..
 
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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...
 
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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...
 
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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..
 
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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..
 
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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..
 
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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..
 
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15

Erken başlangıçlı ve idiyopatik parkinson hastalarında GBA ..:

Anlaş, Özlem
Tez.  , 2017
Link: https://hdl.handle.net/1..
 
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