Keyword: genetic

9 articles found.

Original Article

Parental knowledge and attitudes towards hereditary hearing loss and genetic technology

Safa Alqudah, Alia Alqudah, Maha Zaitoun, Hussein Alqassem

ELECTRON J GEN MED, 2023, Volume 20, Issue 6, Article No: em548

https://doi.org/10.29333/ejgm/13813

Review Article

A new insight updates in diagnosis and management of acute lymphoblastic leukemia, cytogenetics, immunophenotyping, and proteomic profile

Sultan Ayesh Mohammed Saghir

ELECTRON J GEN MED, 2023, Volume 20, Issue 5, Article No: em519

https://doi.org/10.29333/ejgm/13386

Case Report

First trimester recurrent pregnancy loss due to balanced chromosomal translocations in husband: A case report

Tuan Nadrah Naim Tuan Ismail, Noraini Mohamad, Zainab Mat Yudin, Nazihah Mohd Yunus

ELECTRON J GEN MED, 2023, Volume 20, Issue 1, Article No: em440

https://doi.org/10.29333/ejgm/12702

Original Article

Clinical Evaluation of Connexin-26 Gene Mutation in the Development of Hearing Loss in the Kazakh Population

Saule Kudaibergenova, Gulzakhira Djarkinbekova, Abdukhalil Musaev, Abdumannop Abdukayumov, Abdugani Musayev, Ayat Assemov

ELECTRON J GEN MED, 2022, Volume 19, Issue 2, Article No: em356

https://doi.org/10.29333/ejgm/11577

Original Article

COVID-19 Outbreak: Application of Multi-gene Genetic Programming to Country-based Prediction Models

Majid Niazkar, Hamid Reza Niazkar

ELECTRON J GEN MED, 2020, Volume 17, Issue 5, Article No: em247

https://doi.org/10.29333/ejgm/8232

Review Article

Rare but lethal short QT syndrome: most recent understanding of the disease

Mustafa Al Qaysi, Juan Simon Rico-Mesa, William Sovic, Manuel Endo-Carvajal, Auroa Badin

ELECTRON J GEN MED, 2019, Volume 16, Issue 5, Article No: em154

https://doi.org/10.29333/ejgm/108495

Original Article

The prevalence of homozygous MTHFR polymorphism(s) in a Turkish university hospital population that necessitated MTHFR polymorphism investigation

Fatma Gumruk, Gokcen Orgul, Ozlem Akgun Dogan, Atakan Tanacan, Ergun Karaagaoglu, Mehmet Sinan Beksac

ELECTRON J GEN MED, 2018, Volume 15, Issue 4, Article No: em57

https://doi.org/10.29333/ejgm/89674

Case Report

Role of genetics in the Primary Biliary Cirrhosis; with the presentation of the three sisters

Tuncer Temel, Pınar Yildiz, Ayşegül Özakyol

EUR J GEN MED, 2016, Volume 13, Issue 3, 72-73

https://doi.org/10.29333/ejgm/81913

Original Article

The Association Between Polymorphism of Lys198Asn of Endothelin-1 Gene and Arterial Hypertension Risk in Kazakh People

A.U. Dzholdasbekova, A.E. Gaipov

EUR J GEN MED, 2010, Volume 7, Issue 2, 187-191

https://doi.org/10.29333/ejgm/82848