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Cangul, Hakan
63
results:
Search for persons
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Online (63)
Mediatypes
Articles (Online) (22)
OpenAccess-fulltext (41)
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english (57)
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1
Computational analysis of missense filamin-A variants, incl..:
Gerlevik, Umut
;
Saygı, Ceren
;
Cangül, Hakan
...
PLOS ONE. 17 (2022) 5 - p. e0265400 , 2022
Link:
https://doi.org/10.1371/..
?
2
Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital ..:
Aycan, Zehra
;
Cangul, Hakan
;
Muzza, Marina
...
The Journal of Clinical Endocrinology & Metabolism. 102 (2017) 9 - p. 3085-3090 , 2017
Link:
https://doi.org/10.1210/..
?
3
Comprehensive Screening of Eight Known Causative Genes in C..:
Nicholas, Adeline K.
;
Serra, Eva G.
;
Cangul, Hakan
...
The Journal of Clinical Endocrinology & Metabolism. 101 (2016) 12 - p. 4521-4531 , 2016
Link:
https://doi.org/10.1210/..
?
4
Nanoparticle growth and surface chemistry changes in cell-c..:
Kendall, Michaela
;
Hodges, Nikolas J.
;
Whitwell, Harry
..
Philosophical Transactions: Biological Sciences. 370 (2015) 1661 - p. 1-9 , 2015
Link:
http://www.jstor.org/sta..
?
5
Thyroid dyshormonogenesis is mainly caused byTPOmutations i..:
Cangul, Hakan
;
Aycan, Zehra
;
Olivera-Nappa, Alvaro
...
Clinical Endocrinology. 79 (2013) 2 - p. 275-281 , 2013
Link:
https://doi.org/10.1111/..
?
6
Jervell and Lange–Nielsen Syndrome: Homozygous Missense Mut..:
Bostan, Ozlem
;
Temel, Şehime G.
;
Cangül, Hakan
..
Pediatric Cardiology. 34 (2013) 8 - p. 2063-2067 , 2013
Link:
https://doi.org/10.1007/..
?
7
Novel truncating thyroglobulin gene mutations associated wi..:
Cangul, Hakan
;
Boelaert, Kristien
;
Dogan, Murat
...
Endocrine. 45 (2013) 2 - p. 206-212 , 2013
Link:
https://doi.org/10.1007/..
?
8
Turkish perspective of Jervell and Lange-Nielsen syndrome:
Temel, SehimeG
;
Bostan, OzlemM
;
Cangul, Hakan
.
Annals of Indian Academy of Neurology. 16 (2013) 1 - p. 129 , 2013
Link:
https://doi.org/10.4103/..
?
9
Duplication of SOX9 is not a common cause of 46,XX testicul..:
Temel, Sehime G.
;
Cangul, Hakan
Journal of Pediatric Endocrinology and Metabolism. 26 (2013) 1-2 - p. , 2013
Link:
https://doi.org/10.1515/..
?
10
TSHR is the main causative locus in autosomal recessively i..:
Cangul, Hakan
;
Aycan, Zehra
;
Saglam, Halil
...
Journal of Pediatric Endocrinology and Metabolism. 25 (2012) 5-6 - p. , 2012
Link:
https://doi.org/10.1515/..
?
11
Mild and severe congenital primary hypothyroidism in two pa..:
Baş, Veysel Nijat
;
Cangul, Hakan
;
Agladioglu, Sebahat Yilmaz
...
Journal of Pediatric Endocrinology and Metabolism. 25 (2012) 11-12 - p. , 2012
Link:
https://doi.org/10.1515/..
?
12
Erratum: Corrigendum: Mutations in VIPAR cause an arthrogry..:
Cullinane, Andrew R
;
Straatman-Iwanowska, Anna
;
Zaucker, Andreas
...
Nature Genetics. 43 (2011) 3 - p. 277-277 , 2011
Link:
https://doi.org/10.1038/..
?
13
Novel TSHR mutations in consanguineous families with congen..:
Cangul, Hakan
;
Morgan, Neil V.
;
Forman, Julia R.
...
Clinical Endocrinology. 73 (2010) 5 - p. 671-677 , 2010
Link:
https://doi.org/10.1111/..
?
14
Mutations in SLC29A3, Encoding an Equilibrative Nucleoside ..:
Morgan, Neil V.
;
Morris, Mark R.
;
Cangul, Hakan
...
PLoS Genetics. 6 (2010) 2 - p. e1000833 , 2010
Link:
https://doi.org/10.1371/..
?
15
Mutations in VIPAR cause an arthrogryposis, renal dysfuncti..:
Cullinane, Andrew R
;
Straatman-Iwanowska, Anna
;
Zaucker, Andreas
...
Nature Genetics. 42 (2010) 4 - p. 303-312 , 2010
Link:
https://doi.org/10.1038/..
1-15