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Works by Cengiz, F. B.

Results: 3

1

Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.

Published in:

Clinical Genetics, 2008, v. 73, n. 6, p. 554, doi. 10.1111/j.1399-0004.2008.01004.x

By:

Tekin, M.;
Akay, H. Öztürkmen;
Fitoz, S.;
Birnbaum, S.;
Cengiz, F. B.;
Sennaroğlu, L.;
İncesulu, A.;
Konuk, E. B. Yüksel;
Bayrak, A. Hasanefendioğlu;
Şentürk, S.;
Cebeci, İ;
Ütine, G. E.;
Tunçbilek, E.;
Nance, W. E.;
Duman, D.

Publication type:

Article

2

The Effect of p.Arg25Cys Alteration in NKX2-5 on Conotruncal Heart Anomalies: Mutation or Polymorphism?

Published in:

Pediatric Cardiology, 2008, v. 29, n. 1, p. 126, doi. 10.1007/s00246-007-9058-2

By:

Akçaboy, M. İ.;
Cengiz, F. B.;
İnceoğlu, B.;
Uçar, T.;
Atalay, S.;
Tutar, E.;
Tekin, M.

Publication type:

Article

3

Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss.

Published in:

Scientific Reports, 2016, p. 31622, doi. 10.1038/srep31622

By:

Bademci, G.;
Cengiz, F. B.;
Foster II, J.;
Duman, D.;
Sennaroglu, L.;
Diaz-Horta, O.;
Atik, T.;
Kirazli, T.;
Olgun, L.;
Alper, H.;
Menendez, I.;
Loclar, I.;
Sennaroglu, G.;
Tokgoz-Yilmaz, S.;
Guo, S.;
Olgun, Y.;
Mahdieh, N.;
Bonyadi, M.;
Bozan, N.;
Ayral, A.

Publication type:

Article