E-LIB Suche - Ergebnisse für: Temel, Sehime G.

1

Genotype and Phenotype Correlation of Patients with Osteoge..:

Aliyeva, Lamiya ; Ongen, Yasemin Denkboy ; Eren, Erdal...
The Journal of Molecular Diagnostics. , 2024

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

2

Homozygous missense variants in YKT6 result in loss of func..:

Ma, Mengqi ; Ganapathi, Mythily ; Zheng, Yiming...
Genetics in Medicine. 26 (2024) 7 - p. 101125 , 2024

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

3

Determining T and B Cell development by TREC/KREC analysis ..:

Şentürk, Gizem ; Ng, Yuk Yin ; Eltan, Sevgi Bilgiç...
Scandinavian Journal of Immunology. 95 (2022) 3 - p. , 2022

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

4

Nanobubble Ozone Stored in Hyaluronic Acid Decorated Liposo..:

Sabancı, Ahmet Umit ; Erkan Alkan, Perihan ; Mujde, Cem...
International Journal of Nanomedicine. 17 (2022) - p. 351-379 , 2022

Link: https://doi.org/10.2147/..

5

Germline landscape of BRCAs by 7-site collaborations as a B..:

Bisgin, Atil ; Sag, Sebnem Ozemri ; Dogan, Muhammet E....
The Breast. 65 (2022) - p. 15-22 , 2022

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

6

A Homozygous Synonymous Variant Likely Cause of Severe Cili..:

Tuncel, Gulten ; Kaymakamzade, Bahar ; Engindereli, Yeliz..
Genes. 12 (2021) 6 - p. 945 , 2021

Link: https://doi.org/10.3390/..

7

The Story of a Ship Journey, Malaria, and the HBB Gene IVS-..:

Ergoren, Mahmut C. ; Temel, Sehime G. ; Mocan, Gamze.
Global Medical Genetics. 8 (2021) 2 - p. 069-071 , 2021

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

8

European recommendations integrating genetic testing into m..:

on behalf of European Society of Human Genetics, European Council of Legal Medicine, European Society of Cardiology working group on myocardial and pericardial diseases, European Reference Network for rare, low prevalence and complex diseases of the heart (ERN GUARD-Heart), Association for European Cardiovascular Pathology ; Fellmann, Florence ; van El, Carla G....
European Journal of Human Genetics. 27 (2019) 12 - p. 1763-1773 , 2019

Link: https://doi.org/10.1038/..

9

Lysinuric protein intolerance and HOIP deficiency in a boy:..:

Aliyeva, Lamiya ; Erdol, Sahin ; Gorukmez, Orhan...
Journal of Biotechnology. 280 (2018) - p. S20 , 2018

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

10

Identification and characterization of a novel FBN1 gene va..:

Ergoren, Mahmut Cerkez ; Turkgenc, Burcu ; Teralı, Kerem...
Connective Tissue Research. 60 (2018) 2 - p. 146-154 , 2018

Link: https://doi.org/10.1080/..

11

Homozygous, and compound heterozygous mutation in 3 Turkish..:

Uysal, Fahrettin ; Turkgenc, Burcu ; Toksoy, Guven...
BMC Medical Genetics. 18 (2017) 1 - p. , 2017

Link: https://doi.org/10.1186/..

12

A Novel TBX19 Gene Mutation in a Case of Congenital Isolate..:

Akcan, Nese ; Serakıncı, Nedime ; Turkgenc, Burcu...
Frontiers in Endocrinology. 8 (2017) - p. , 2017

Link: https://doi.org/10.3389/..

13

Duplication of SOX9 is not a common cause of 46,XX testicul..:

Temel, Sehime G. ; Cangul, Hakan
Journal of Pediatric Endocrinology and Metabolism. 26 (2013) 1-2 - p. , 2013

Link: https://doi.org/10.1515/..

14

Jervell and Lange–Nielsen Syndrome: Homozygous Missense Mut..:

Bostan, Ozlem ; Temel, Şehime G. ; Cangül, Hakan..
Pediatric Cardiology. 34 (2013) 8 - p. 2063-2067 , 2013

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

15

Microwave-assisted antigen retrieval and incubation with co..:

Temel, Sehime G. ; Minbay, F. Zehra ; Kahveci, Zeynep.
Journal of Neuroscience Methods. 156 (2006) 1-2 - p. 154-160 , 2006

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