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Saudi Medical Journal
|
April 20, 2025
Advancing genetic counselling in Southern Africa: Unveiling opportunities for inclusive healthcare and genomic education for Angola
Maria Chimpolo, Shahida Moosa, Catherine Lynn T Silao, et al.
BMC Research Notes
|
February 27, 2016
Harmonizing the interpretation of genetic variants across the world: the Malaysian experience
Nik Norliza Nik Hassan, John-Paul Plazzer, Timothy D Smith, et al.
Asian Biomedicine : Research, Reviews and News
|
August 8, 2023
Central resources of variant discovery and annotation and its role in precision medicine
Hashim Halim-Fikri, Sharifah-Nany Rahayu-Karmilla Syed-Hassan, Wan-Khairunnisa Wan-Juhari, et al.
Human Mutation
|
September 12, 2021
Adapting the ACMG/AMP variant classification framework: A perspective from the ClinGen Hemoglobinopathy Variant Curation Expert Panel
Petros Kountouris, Coralea Stephanou, Carsten W Lederer, et al.
Elife
|
December 1, 2022
Evaluation of in silico predictors on short nucleotide variants in <i>HBA1</i>, <i>HBA2</i>, and <i>HBB</i> associated with haemoglobinopathies
Stella Tamana, Maria Xenophontos, Anna Minaidou, et al.
Database : the Journal of Biological Databases and Curation
|
September 4, 2024
Global Globin Network and adopting genomic variant database requirements for thalassemia
Hashim Halim-Fikri, Ninie Nadia Zulkipli, Hafiza Alauddin, et al.
BMC Research Notes
|
May 1, 2015
The first Malay database toward the ethnic-specific target molecular variation
Hashim Halim-Fikri, Ali Etemad, Ahmad Zubaidi Abdul Latif, et al.
Journal of Personalized Medicine
|
April 23, 2022
Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries
Bin Hashim Halim-Fikri, Carsten W Lederer, Atif Amin Baig, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Saudi Medical Journal
|
April 20, 2025
Advancing genetic counselling in Southern Africa: Unveiling opportunities for inclusive healthcare and genomic education for Angola
Maria Chimpolo, Shahida Moosa, Catherine Lynn T Silao, et al.
BMC Research Notes
|
February 27, 2016
Harmonizing the interpretation of genetic variants across the world: the Malaysian experience
Nik Norliza Nik Hassan, John-Paul Plazzer, Timothy D Smith, et al.
Asian Biomedicine : Research, Reviews and News
|
August 8, 2023
Central resources of variant discovery and annotation and its role in precision medicine
Hashim Halim-Fikri, Sharifah-Nany Rahayu-Karmilla Syed-Hassan, Wan-Khairunnisa Wan-Juhari, et al.
Human Mutation
|
September 12, 2021
Adapting the ACMG/AMP variant classification framework: A perspective from the ClinGen Hemoglobinopathy Variant Curation Expert Panel
Petros Kountouris, Coralea Stephanou, Carsten W Lederer, et al.
Elife
|
December 1, 2022
Evaluation of in silico predictors on short nucleotide variants in <i>HBA1</i>, <i>HBA2</i>, and <i>HBB</i> associated with haemoglobinopathies
Stella Tamana, Maria Xenophontos, Anna Minaidou, et al.
Database : the Journal of Biological Databases and Curation
|
September 4, 2024
Global Globin Network and adopting genomic variant database requirements for thalassemia
Hashim Halim-Fikri, Ninie Nadia Zulkipli, Hafiza Alauddin, et al.
BMC Research Notes
|
May 1, 2015
The first Malay database toward the ethnic-specific target molecular variation
Hashim Halim-Fikri, Ali Etemad, Ahmad Zubaidi Abdul Latif, et al.
Journal of Personalized Medicine
|
April 23, 2022
Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries
Bin Hashim Halim-Fikri, Carsten W Lederer, Atif Amin Baig, et al.
Page
of 1