Works by Tunçbilek, E.

Results: 10

Anaemia and thrombocytopenia due to haemophagocytosis in a 7-month-old boy with galactosialidosis.

Published in:

Journal of Inherited Metabolic Disease, 1998, v. 21, n. 6, p. 679, doi. 10.1023/A:1005444903597

By:

Olcay, L.;
Gümrük, F.;
Boduroğlu, K.;
Coşkun, T.;
Tunçbilek, E.

Publication type:

Article

No Evidence for Overexpression of the p53 Protein and Mutations in Exons 4-9 of the p53 Gene in a Large Family With Adenomatous Polyposis.

Published in:

American Journal of Gastroenterology (Springer Nature), 1998, v. 93, n. 9, p. 1524, doi. 10.1016/S0002-9270(98)00295-0

By:

Aktas, D.;
Ayhan, A.;
Tunçbilek, E.;
Özdemir, A.;
Uzunalimoglu, B.

Publication type:

Article

Indicators of nutritional status in Turkish preschool children: results of Turkish Demographic and Health Survey 1993.

Published in:

1996

By:

Tunçbilek, Ergül;
Ünalan, Turgay;
Coşkun, Turgay;
Tunçbilek, E;
Unalan, T;
Coşkun, T

Publication type:

journal article

Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability.

Published in:

Molecular Syndromology, 2012, v. 2, n. 2, p. 64, doi. 10.1159/000334289

By:

Utine, G.E.;
Kiper, P.Ö.;
Alanay, Y.;
Haliloğlu, G.;
Aktaş, D.;
Boduroğlu, K.;
Tunçbilek, E.;
Alikaşifoğlu, M.

Publication type:

Article

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

High frequency hearing loss in Ullrich-Turner syndrome.

Published in:

2000

By:

Güngör, Neslihan;
Böke, Bilgehan;
Belgin, Erol;
Tuncbilek, Ergül;
Güngör, N;
Böke, B;
Belgin, E;
Tunçbilek, E

Publication type:

journal article

Prenatal diagnosis of laryngeal atresia.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 4, p. 277

By:

L. Önderoǧlu;
B. Saygan Karamürsel;
A. Bulun;
G. Kale;
E. Tunçbilek

Publication type:

Article

A multidisciplinary approach to the management of individuals with fragile X syndrome.

Published in:

Journal of Intellectual Disability Research, 2007, v. 51, n. 2, p. 151, doi. 10.1111/j.1365-2788.2006.00942.x

By:

Alanay, Y.;
Ünal, F.;
Turanlı, G.;
Alikaşifoğlu, M.;
Alehan, D.;
Akyol, U.;
Belgin, E.;
Şener, C.;
Aktaş, D.;
Boduroğlu, K.;
Utine, E.;
Volkan‐Salancı, B.;
Özusta, Ş.;
Genç, A.;
Başar, F.;
Sevinç, Ş.;
Tunçbilek, E.

Publication type:

Article

Perinatal mortality rate hospital based study during 19982001 at Hacettepe University.

Published in:

Journal of Perinatal Medicine, 2003, v. 31, n. 5, p. 435

By:

PERINATALMORTALITY STUDY GROUP: T. DURUKAN;
L. öNDEROGLU;
ö. DEREN;
B. SAYGAN-KARAMüRSEL;
G. ERDEM;
O. ORAM;
M. GüLSEVIN;
S. YURDAKöK;
S. öZKUTLU;
A. çELIKER;
G. KALE;
M. çAGLAR;
S. GüçER;
A. BULUN;
B.TALIM;
N. BüYüKPAMUKçU;
A. çIFTÇI;
E. TUNçBILEK;
S. BALCI;
Y. ALANAY

Publication type:

Article

Benefit of high-dose methylprednisolone in comparison with conventional-dose prednisolone during remission induction therapy in childhood acute lymphoblastic leukemia for long-term follow-up.

Published in:

Leukemia (08876924), 2003, v. 17, n. 2, p. 328, doi. 10.1038/sj.leu.2402673

By:

Yetgin, S;
Tuncer, M A;
Çetin, M;
Gümrük, F;
Yenicesu, I;
Tunç, B;
Öner, A F;
Toksoy, H;
Koç, A;
Aslan, D;
Özyürek, E;
Olcay, L;
Atahan, L;
Tunçbilek, E;
Gürgey, A

Publication type:

Article