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Akata, Rüştü Fikret
8  results:
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1

The search for new approaches to treating type 1 plasminoge..:

Aslan, Deniz ; Akata, Rüştü Fikret
Pediatric Blood & Cancer.  65 (2017)  4 - p. , 2017
Link: https://doi.org/10.1002/..
 
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2

Oculoectodermal syndrome: Report of a new case with a broad..:

Aslan, Deniz ; Akata, Rustu Fikret ; Schröder, Julia...
American Journal of Medical Genetics Part A.  164 (2014)  11 - p. 2947-2951 , 2014
Link: https://doi.org/10.1002/..
 
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3

Dyskeratosis congenita and limbal stem cell deficiency:

Aslan, Deniz ; Akata, Rustu Fikret
Experimental Eye Research.  90 (2010)  3 - p. 472-473 , 2010
Link: https://doi.org/10.1016/..
 
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4

Homozygous OB-fold variants in telomere protein TPP1 are as..:

Akata, Rüştü Fikret ; Aslan, Deniz ; Vulliamy, Tom...
c31d0629-f448-41ba-a86b-c9b50a05b2d1.  , 2018
Link: https://doi.org/10.1182/..
 
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5

Genetic Analysis Of Chst6 And Tgfbi In Turkish Patients Wit..:

Yaylacioglu Tuncay, Fulya ; Kayman Kurekci, Gülsüm ; Guntekin Ergun, Sezen...
Molecular Vision.  , 2016
Link: http://hdl.handle.net/11..
 
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6

Genetic analysis of CHST6 and TGFBI in Turkish patients wit..:

Tuncay, Fulya Yaylacioglu ; Kurekci, Gulsum Kayman ; Ergun, Sezen Guntekin...
https://aperta.ulakbim.gov.tr/record/111696.  , 2016
Link: https://aperta.ulakbim.g..
 
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7

Homozygous OB-fold variants in telomere protein TPP1 are as..:

Tummala, Hemanth ; Collopy, Laura C ; Walne, Amanda J...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6293869/.  , 2018
Link: http://www.ncbi.nlm.nih...
 
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8

Limbal stem cell deficiency in patients with inherited stem..:

Aslan, Deniz ; Akata, Rustu F. ; Holme, Harriet..
International Ophthalmology.  32 (2012)  6 - p. 615-622 , 2012
Link: https://doi.org/10.1007/..
 
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