E-LIB Suche - Ergebnisse für: Zeybek, Selcan

1

Severe microcephaly and rapid deterioration due to cortical..:

Olmez, Akgun ; Zeybek, Selcan
Annals of Indian Academy of Neurology. 25 (2022) 4 - p. 735 , 2022

Link: https://doi.org/10.4103/..

2

A Novel Homozygous GALK1 Variant Combined With Cataract and..:

Ozler, Oguz ; Egeli, Bugra Han ; Zeybek, Selcan..
Clinical Pediatrics. 62 (2022) 6 - p. 537-540 , 2022

Link: https://doi.org/10.1177/..

3

Further delineation of ACPHD syndrome and a novel mutation ..:

Öztürk, Menekşe ; Zeybek, Selcan ; Farre, G...
EUROPEAN JOURNAL OF HUMAN GENETICS. , 2019

Link: https://hdl.handle.net/1..

4

A Novel Nonsense Mutation In The EYA1 Gene Found In A Patie..:

Albuz, Burcu ; Zeybek, Selcan ; Anlas, Özlem...
EUROPEAN JOURNAL OF HUMAN GENETICS. , 2019

Link: https://hdl.handle.net/1..

5

The co-existence of Nablus Mask-Like Facial Syndrome and Kl..:

Anlaş, Özlem ; Sarikepe, B ; Zeybek, Selcan...
EUROPEAN JOURNAL OF HUMAN GENETICS. , 2019

Link: https://hdl.handle.net/1..

6

Co-existence of Goldenhar and Klinefelter Syndromes in a Pa..:

Zeybek, Selcan ; Sarıkepe, Bilge ; Bağcı, Gülseren..
Erciyes Medical Journal. , 2018

Link: https://hdl.handle.net/1..

7

Familial mutation in caffey disease with reduced penetrance..:

Özdemir, Özmert Muhammet Ali ; Tancer-Elçi, Hazal ; Polat, Aziz...
Turkish Journal of Pediatrics. , 2017

Link: https://hdl.handle.net/1..

8

Familial mutation in Caffey disease with reduced penetrance..:

Ayaz, Akif ; Özdemir, Özmert M. A ; Tancer-Elçi, Hazal...
Turkish Journal of Pediatrics. , 2016

Link: https://hdl.handle.net/1..

9

Tekrarlayan gebelik kaybı olan vakalarda pentraxin 3 ekspre..:

Zeybek, Selcan
Tez. , 2015

Link: https://hdl.handle.net/1..

10

Severe microcephaly and rapid deterioration due to cortical..:

Akgun Olmez ; Selcan Zeybek
http://www.annalsofian.org/article.asp?issn=0972-2327;year=2022;volume=25;issue=4;spage=735;epage=738;aulast=Olmez. , 2022

Link: https://doi.org/10.4103/..