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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

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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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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11

Structural, Functional, and Clinical Characterization of a ..:

Pannone, Luca ; Bocchinfuso, Gianfranco ; Flex, Elisabetta...
Human Mutation.  38 (2017)  4 - p. 451-459 , 2017
Link: https://doi.org/10.1002/..
 
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12

Cover Image, Volume 38, Issue 4:

Pannone, Luca ; Bocchinfuso, Gianfranco ; Flex, Elisabetta...
Human Mutation.  38 (2017)  4 - p. i-i , 2017
Link: https://doi.org/10.1002/..
 
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13

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/..
 
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14

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/..
 
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15

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/..
 
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