E-LIB Suche - Ergebnisse für: Atli, Engin

1

A Study of FoxO1, mTOR, miR-21, miR-29b, and miR-98 Express..:

Akdağ, Nazan ; Atli, Engin ; Zhuri̇, Drenushe..
Cureus. , 2024

Link: https://doi.org/10.7759/..

2

The Frequency of SMN1, SMN2 Copy Numbers in 246 Turkish Cas..:

Yalcintepe, Sinem ; Karal, Yasemin ; Demir, Selma...
Global Medical Genetics. 10 (2023) 2 - p. 117-122 , 2023

Link: https://doi.org/10.1055/..

3

Investigation of Relationship Between Small Noncoding RNA (..:

Ay, Arzu ; Alkanli, Nevra ; Atli, Engin...
Molecular Neurobiology. 60 (2022) 2 - p. 875-883 , 2022

Link: https://doi.org/10.1007/..

4

Investigation on the Effects of Modifying Genes on the Spin..:

Zhuri, Drenushe ; Gurkan, Hakan ; Eker, Damla...
Global Medical Genetics. 9 (2022) 3 - p. 226-236 , 2022

Link: https://doi.org/10.1055/..

5

Investigating the Genetic Etiology of Pediatric Patients wi..:

Eker, Damla ; Gurkan, Hakan ; Karal, Yasemin...
Global Medical Genetics. 9 (2022) 3 - p. 200-207 , 2022

Link: https://doi.org/10.1055/..

6

Prenatal diagnosis and molecular cytogenetic characterizati..:

Atli, Emine Ikbal ; Atli, Engin ; Inan, Cihan...
Taiwanese Journal of Obstetrics and Gynecology. 61 (2022) 3 - p. 504-509 , 2022

Link: https://doi.org/10.1016/..

7

Customised targeted massively parallel sequencing enables m..:

Atli, Emine Ikbal ; Atli, Engin ; Yalcintepe, Sinem...
Internal Medicine Journal. 52 (2022) 7 - p. 1174-1184 , 2022

Link: https://doi.org/10.1111/..

8

Investigation of Genes Associated With Atherosclerosis in P..:

BALCI, Mehmet Ali ; ATLI, Engin ; GüRKAN, Hakan
Archives of Rheumatology. 36 (2021) 2 - p. 287-295 , 2021

Link: https://doi.org/10.46497..

9

Germline Pathogenic Variants Identified by Targeted Next-Ge..:

Yalcintepe, Sinem ; Gurkan, Hakan ; Korkmaz, Fatma Nur...
Journal of Kidney Cancer and VHL. 8 (2021) 1 - p. 19-24 , 2021

Link: https://doi.org/10.15586..

10

Clinical Features of Aberrations Chromosome 22q: A Pilot St..:

Atli, Emine Ikbal ; Atli, Engin ; Yalcintepe, Sinem...
Global Medical Genetics. 9 (2021) 1 - p. 042-050 , 2021

Link: https://doi.org/10.1055/..

11

Prenatal diagnosis of 20p13 microdeletion syndrome:

Yener, Cem ; Sayın, Cenk ; İnan, Cihan...
Taiwanese Journal of Obstetrics and Gynecology. 60 (2021) 2 - p. 350-354 , 2021

Link: https://doi.org/10.1016/..

12

Investigation of Genetic Alterations in Congenital Heart Di..:

Atli, Emine Ikbal ; Atli, Engin ; Yalcintepe, Sinem...
Global Medical Genetics. 9 (2021) 1 - p. 029-033 , 2021

Link: https://doi.org/10.1055/..

13

Investigation the etiology of syndromic autism with targete..:

Yalcintepe, Sinem ; Gurkan, Hakan ; Demir, Selma...
Annals of Medical Research. 28 (2021) 12 - p. 2174 , 2021

Link: https://doi.org/10.5455/..

14

A Child with 5q Deletion and Accompanying Chiari 1 Malforma..:

Atli, Emine Ikbal ; Yalcintepe, Sinem ; Atli, Engin..
The Indian Journal of Pediatrics. 87 (2020) 9 - p. 766-766 , 2020

Link: https://doi.org/10.1007/..

15

Two Novel Pathogenic FBN1 Variations and Their Phenotypic R..:

Yalcintepe, Sinem ; Demir, Selma ; Atli, Emine Ikbal...
Global Medical Genetics. 7 (2020) 2 - p. 068-071 , 2020

Link: https://doi.org/10.1055/..