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Karaer, Kadri
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1

Filippi syndrome: Three new families suggest that urinary s..:

Bas, Hasan ; Durmaz, Ceren Damla ; Tombak, Merve Celenkoglu..
American Journal of Medical Genetics Part A.  , 2024
Link: https://doi.org/10.1002/..
 
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2

Evaluation of the frequency of MEFV gene variants in patien..:

Karaer, Derya ; Şahinoğlu, B ; Gürler, A.İ.
Pamukkale Medical Journal.  , 2023
Link: https://hdl.handle.net/1..
 
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3

The Molecular Spectrum of Beta Thalassemia Mutations in Sou..:

Karaer, Derya ; Şahinoğlu, Bahtiyar ; Şahinoğlu, Esra Pekpak...
Gazi Medical Journal.  , 2023
Link: https://hdl.handle.net/1..
 
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4

Two novel variants in SCARF2 gene underlie van den Ende‐Gup..:

Karaer, Derya ; Karaer, Kadri
American Journal of Medical Genetics Part A.  188 (2022)  6 - p. 1881-1884 , 2022
Link: https://doi.org/10.1002/..
 
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5

Early onset disease, anarthria, areflexia, and dystonia can..:

Ölmez, Akgün ; Çetin, Gökhan Ozan ; Karaer, Kadri
American Journal of Medical Genetics Part A.  188 (2022)  9 - p. 2712-2717 , 2022
Link: https://doi.org/10.1002/..
 
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6

Two novel variants in SCARF2 gene underlie van den Ende-Gup..:

Karaer, Kadri ; Karaer, Derya
American Journal Of Medical Genetics Part A.  , 2022
Link: https://hdl.handle.net/1..
 
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7

Targeted next-generation sequencing (NGS) analysis of mutat..:

Keskin, Gul ; Ucar Gundogar, Zubeyde ; Karaer, Kadri
Journal Of Orofacial Orthopedics-Fortschritte Der Kieferorthopadie.  , 2022
Link: https://hdl.handle.net/1..
 
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8

Early onset disease, anarthria, areflexia, and dystonia can..:

Olmez, Akgun ; Cetin, Gokhan Ozan ; Karaer, Kadri
American Journal Of Medical Genetics Part A.  , 2022
Link: https://hdl.handle.net/1..
 
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9

Investigating consanguineous families from Turkey to identi..:

Gumuslu, Esen ; Guemues, Evren ; Oz, Ozlem...
European Journal Of Human Genetics.  , 2022
Link: https://hdl.handle.net/1..
 
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10

From cataract to syndrome diagnosis: Revaluation of Warburg..:

Mutlu Albayrak, Hatice ; Elçioğlu, Nursel H. ; Yeter, Burcu.
American Journal of Medical Genetics Part A.  185 (2021)  8 - p. 2325-2334 , 2021
Link: https://doi.org/10.1002/..
 
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11

Targeted next-generation sequencing (NGS) analysis of mutat..:

Keskin, Gül ; Karaer, Kadri ; Uçar Gündoğar, Zübeyde
Journal of Orofacial Orthopedics / Fortschritte der Kieferorthopädie.  83 (2021)  S1 - p. 65-74 , 2021
Link: https://doi.org/10.1007/..
 
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12

İnfertil erkek hastalarda karyotip analizi ve Y kromozom mi..:

Gürler, Abdullah İhsan ; Şahinoğlu, Bahtiyar ; Kadri Karaer
Pamukkale Tıp Dergisi.  , 2021
Link: https://hdl.handle.net/1..
 
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13

From cataract to syndrome diagnosis: Revaluation of Warburg..:

Mutlu Albayrak, Hatice ; Elçioğlu, Nursel H ; Yeter, Burcu.
American Journal of Medical Genetics, Part A.  , 2021
Link: https://hdl.handle.net/1..
 
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14

VDR gene polymorphisms as a significant factor in unexplain..:

Isbilen, Elif ; Ulusal, Hasan ; Karaer, Kadri...
Gene Reports.  21 (2020)  - p. 100962 , 2020
Link: https://doi.org/10.1016/..
 
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15

A case of de novo microdeletion with combination of 1q21.1 ..:

Hale Onder Yilmaz ; Kadri Karaer ; Orkun Yilmaz
http://www.ejmanager.com/fulltextpdf.php?mno=116442.  , 2020
Link: https://doi.org/10.24911..
 
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