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Karaer, Kadri
50
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Online (50)
Mediatypes
Articles (Online) (22)
OpenAccess-fulltext (28)
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english (46)
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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/..
?
2
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/..
?
3
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/..
?
4
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/..
?
5
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/..
?
6
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/..
?
7
Phenotypic spectrum associated with SPECC1L pathogenic vari..:
Bhoj, Elizabeth J.
;
Haye, Damien
;
Toutain, Annick
...
European Journal of Medical Genetics. 62 (2019) 12 - p. 103588 , 2019
Link:
https://doi.org/10.1016/..
?
8
Vocal cord immobility as a cause of aphonia in a child with..:
Mutlu-Albayrak, Hatice
;
Karaer, Kadri
International Journal of Pediatric Otorhinolaryngology. 117 (2019) - p. 179-181 , 2019
Link:
https://doi.org/10.1016/..
?
9
Unusual hair findings in a child with cardiofaciocutaneous ..:
Işikay, Sedat
;
Karaer, Kadri
International Journal of Dermatology. 58 (2018) 3 - p. 354-356 , 2018
Link:
https://doi.org/10.1111/..
?
10
Novel mutations in the LRP5 gene in patients with Osteoporo..:
Pekkinen, Minna
;
Grigelioniene, Giedre
;
Akin, Leyla
...
American Journal of Medical Genetics Part A. 173 (2017) 12 - p. 3132-3135 , 2017
Link:
https://doi.org/10.1002/..
?
11
Novel mutation in SUCLA2 identified on sequencing analysis:
Güngör, Olcay
;
Özkaya, Ahmet Kağan
;
Güngör, Gülay
...
Pediatrics International. 58 (2016) 7 - p. 659-661 , 2016
Link:
https://doi.org/10.1111/..
?
12
Early-Onset Mild Type Leukoencephalopathy Caused by a Homoz..:
Taskin, Birce Dilge
;
Karalok, Zeynep Selen
;
Gurkas, Esra
...
Journal of Child Neurology. 31 (2016) 7 - p. 938-941 , 2016
Link:
https://doi.org/10.1177/..
?
13
Familial cardiofaciocutaneous syndrome in a father and a so..:
Karaer, Kadri
;
Lissewski, Christina
;
Zenker, Martin
American Journal of Medical Genetics Part A. 167 (2014) 2 - p. 385-388 , 2014
Link:
https://doi.org/10.1002/..
?
14
Gorlin–chaudhry–moss syndrome revisited: Expanding the phen..:
Rosti, Rasim O.
;
Karaer, Kadri
;
Karaman, Birsen
...
American Journal of Medical Genetics Part A. 161 (2013) 7 - p. 1737-1742 , 2013
Link:
https://doi.org/10.1002/..
?
15
A new nonsense mutation in the NF1 gene with neurofibromato..:
Yimenicioğlu, Sevgi
;
Yakut, Ayten
;
Karaer, Kadri
...
Child's Nervous System. 28 (2012) 12 - p. 2181-2183 , 2012
Link:
https://doi.org/10.1007/..
1-15