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Cengiz, Filiz Basak
149
results:
Online X
Format
Online (149)
Mediatypes
Articles (Online) (116)
Bookchapter (Online) (1)
OpenAccess-fulltext (32)
Sorted by: Relevance
Sorted by: Year
?
1
Dysfunction ofGRAP, encoding the GRB2-related adaptor prote..:
Li, Chong
;
Bademci, Guney
;
Subasioglu, Asli
...
Proceedings of the National Academy of Sciences. 116 (2019) 4 - p. 1347-1352 , 2019
Link:
https://doi.org/10.1073/..
?
2
Dysfunction of GRAP, encoding the GRB2-related adaptor prot..:
Li, Chong
;
Bademci, Guney
;
Subasioglu, Asli
...
Proceedings of the National Academy of Sciences of the United States of America. 116 (2019) 4 - p. 1347-1352 , 2019
Link:
https://www.jstor.org/st..
?
3
Monosomy chromosome 21 compensated by 21q22.11q22.3 duplica..:
Su, Meng
;
Benke, Paul J.
;
Bademci, Guney
...
Molecular Cytogenetics. 11 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
4
Ripor2 is involved in auditory hair cell stereociliary bund..:
Diaz-Horta, Oscar
;
Abad, Clemer
;
Cengiz, Filiz Basak
...
Journal of Molecular Medicine. 96 (2018) 11 - p. 1227-1238 , 2018
Link:
https://doi.org/10.1007/..
?
5
Identification of candidate gene FAM183A and novel pathogen..:
McSherry, Megan
;
Masih, Katherine E.
;
Elcioglu, Nursel H.
...
PLOS ONE. 13 (2018) 11 - p. e0208324 , 2018
Link:
https://doi.org/10.1371/..
?
6
Dominant deafness–onychodystrophy syndrome caused by an ATP..:
Menendez, Ibis
;
Carranza, Claudia
;
Herrera, Mariana
...
Clinical Case Reports. 5 (2017) 4 - p. 376-379 , 2017
Link:
https://doi.org/10.1002/..
?
7
Novel pathogenic variants underlie SLC26A4 -related hearing..:
Cengiz, Filiz Basak
;
Yilmazer, Rasim
;
Olgun, Levent
...
International Journal of Pediatric Otorhinolaryngology. 101 (2017) - p. 167-171 , 2017
Link:
https://doi.org/10.1016/..
?
8
Novel EYA1 variants causing Branchio-oto-renal syndrome:
Klingbeil, Kyle D.
;
Greenland, Christopher M.
;
Arslan, Selcuk
...
International Journal of Pediatric Otorhinolaryngology. 98 (2017) - p. 59-63 , 2017
Link:
https://doi.org/10.1016/..
?
9
Audiological findings in Noonan syndrome:
Tokgoz-Yilmaz, Suna
;
Turkyilmaz, Meral Didem
;
Cengiz, Filiz Basak
...
International Journal of Pediatric Otorhinolaryngology. 89 (2016) - p. 50-54 , 2016
Link:
https://doi.org/10.1016/..
?
10
Correction: Whole-Exome Sequencing Efficiently Detects Rare..:
Diaz-Horta, Oscar
;
Duman, Duygu
;
Foster, Joseph
...
PLoS ONE. 8 (2013) 5 - p. , 2013
Link:
https://doi.org/10.1371/..
?
11
Whole-Exome Sequencing Efficiently Detects Rare Mutations i..:
Diaz-Horta, Oscar
;
Duman, Duygu
;
Foster, Joseph
...
PLoS ONE. 7 (2012) 11 - p. e50628 , 2012
Link:
https://doi.org/10.1371/..
?
12
GJB2 Mutations in Mongolia: Complex Alleles, Low Frequency,..:
Tekin, Mustafa
;
Xia, Xia‐Juan
;
Erdenetungalag, Radnaabazar
...
Annals of Human Genetics. 74 (2010) 2 - p. 155-164 , 2010
Link:
https://doi.org/10.1111/..
?
13
A FGF3 mutation associated with differential inner ear malf..:
Ramsebner, Reinhard
;
Ludwig, Martin
;
Parzefall, Thomas
...
The Laryngoscope. 120 (2009) 2 - p. 359-364 , 2009
Link:
https://doi.org/10.1002/..
?
14
Mutations in TMC1 contribute significantly to nonsyndromic ..:
Sırmacı, Aslı
;
Duman, Duygu
;
Öztürkmen-Akay, Hatice
...
International Journal of Pediatric Otorhinolaryngology. 73 (2009) 5 - p. 699-705 , 2009
Link:
https://doi.org/10.1016/..
?
15
Familial neonatal Marfan syndrome due to parental mosaicism..:
Tekin, Mustafa
;
Cengiz, Filiz Başak
;
Ayberkin, Eda
...
American Journal of Medical Genetics Part A. 143A (2007) 8 - p. 875-880 , 2007
Link:
https://doi.org/10.1002/..
1-15