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Rare coinheritance of hemoglobin vancleave with severe beta-thalassemia mutation in a patient with secondary erythrocytosis.
Hum Genome Var. 2024 Apr 23;11(1):19. doi: 10.1038/s41439-024-00275-y.
Hum Genome Var. 2024.
PMID: 38653961
Free PMC article.
Characterization of New Alpha Zero (α0) Thalassaemia Deletion (--GB) among Malays in Malaysian Population.
Yasin NM, Abdul Hamid FS, Hassan S, Mat Yusoff Y, Mohd Sahid EN, Esa E.
Yasin NM, et al. Among authors: abdul hamid fs.
Diagnostics (Basel). 2023 Oct 23;13(20):3286. doi: 10.3390/diagnostics13203286.
Diagnostics (Basel). 2023.
PMID: 37892108
Free PMC article.
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Next-Generation Sequencing (NGS) and Third-Generation Sequencing (TGS) for the Diagnosis of Thalassemia.
Hassan S, Bahar R, Johan MF, Mohamed Hashim EK, Abdullah WZ, Esa E, Abdul Hamid FS, Zulkafli Z.
Hassan S, et al. Among authors: abdul hamid fs.
Diagnostics (Basel). 2023 Jan 19;13(3):373. doi: 10.3390/diagnostics13030373.
Diagnostics (Basel). 2023.
PMID: 36766477
Free PMC article.
Review.
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Molecular and hematological studies in a cohort of beta zero South East Asia deletion (β°-thal SEA) from Malaysian perspective.
Yasin NM, Abdul Hamid FS, Hassan S, Sudin A, Yassim H, Mohd Sahid EN, Mat Yusoff Y, Esa E, Saleem M.
Yasin NM, et al. Among authors: abdul hamid fs.
Front Pediatr. 2022 Nov 30;10:974496. doi: 10.3389/fped.2022.974496. eCollection 2022.
Front Pediatr. 2022.
PMID: 36533237
Free PMC article.
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Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies.
Tamana S, Xenophontos M, Minaidou A, Stephanou C, Harteveld CL, Bento C, Traeger-Synodinos J, Fylaktou I, Yasin NM, Abdul Hamid FS, Esa E, Halim-Fikri H, Zilfalil BA, Kakouri AC; ClinGen Hemoglobinopathy Variant Curation Expert Panel; Kleanthous M, Kountouris P.
Tamana S, et al. Among authors: abdul hamid fs.
Elife. 2022 Dec 1;11:e79713. doi: 10.7554/eLife.79713.
Elife. 2022.
PMID: 36453528
Free PMC article.
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An insight of -50 (G>A) mutation in the direct repeat element of the β-globin gene: From Malaysian perspective.
Mohd Yasin N, Abdul Hamid FS, Hassan S, Mat Yusoff Y, Mohd Sahid EN, Esa E.
Mohd Yasin N, et al. Among authors: abdul hamid fs.
Malays J Pathol. 2022 Aug;44(2):301-302.
Malays J Pathol. 2022.
PMID: 36043595
Free article.
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Rare cause of transfusion-dependent hemolytic anemia: A case report of HbE/Hb Nottingham and literature review.
Aziz A, Baharin MF, Fauzi MY, Abdul Hamid FS, Nadarajaw T, Ahmad R, Hashim H.
Aziz A, et al. Among authors: abdul hamid fs.
Pediatr Blood Cancer. 2022 Sep;69(9):e29629. doi: 10.1002/pbc.29629. Epub 2022 Mar 6.
Pediatr Blood Cancer. 2022.
PMID: 35253358
Review.
No abstract available.
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