Detection of β-Thalassemia Mutations Using TaqMan Single Nucleotide Polymorphism Genotyping Assays-Reference-Cited by-同舟云学术

Detection of β-Thalassemia Mutations Using TaqMan Single Nucleotide Polymorphism Genotyping Assays

Published:2016-03 Issue:3 Volume:20 Page:154-157
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Alwazani Wissam A.¹²,Zahid Rawabi¹,Elaimi Aisha¹³,Bajouh Osamah¹⁴,Hindawi Salwa⁴,Arab Badr⁴,Damanhouri Ghazi²⁴,Saka Mohamad Yassin²,Turki Rola⁴,Khan Jalaluddin A.⁵,Dallol Ashraf¹⁶,Abuzenadah Adel M.¹³⁶

Affiliation:

1. Center of Innovation in Personalized Medicine, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.

2. King Fahad Medical Research Center, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.

3. Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.

4. King Abdulaziz University Hospital, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.

5. Department of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.

6. Center of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2015.0222

Reference11 articles.

1. Molecular Basis of β-Thalassemia in the Western Province of Saudi Arabia: Identification of Rare β-Thalassemia Mutations

2. Molecular Bases ofβ-Thalassemia in the Eastern Province of Saudi Arabia

3. Homozygosity for the Severe β+-Thalassemia Mutation [IVS-I-5 (G>C)] Causes the Phenotype of Thalassemia Trait: An Extremely Rare Presentation

4. Comprehensive and EfficientHBBMutation Analysis for Detection of β-Hemoglobinopathies in a Pan-Ethnic Population

5. Molecular Diagnostic Challenges of the Thalassemias

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1. Postnatal and non-invasive prenatal detection of β-thalassemia mutations based on Taqman genotyping assays;PLOS ONE;2017-02-24