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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2022 | 3 |
2023 | 3 |
2024 | 1 |
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Page 1
Next-Generation Sequencing (NGS) and Third-Generation Sequencing (TGS) for the Diagnosis of Thalassemia.
Diagnostics (Basel). 2023 Jan 19;13(3):373. doi: 10.3390/diagnostics13030373.
Diagnostics (Basel). 2023.
PMID: 36766477
Free PMC article.
Review.
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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Clinical and haematological characteristics of 38 individuals with Hb G-Makassar in Malaysia.
Esa E, Mohamad AS, Hamzah R, Hamid FSA, Aziz NA, Sevaratnam V, Sathar J, Chen G, Yasin NM.
Esa E, et al. Among authors: hamid fsa.
EJHaem. 2023 Aug 10;4(4):940-948. doi: 10.1002/jha2.750. eCollection 2023 Nov.
EJHaem. 2023.
PMID: 38024609
Free PMC article.
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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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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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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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Rare coinheritance of hemoglobin vancleave with severe beta-thalassemia mutation in a patient with secondary erythrocytosis.
Aziz NA, Musa NH, Mathews M, Rajenderan KT, Abdul Hamid FS, Hassan S, Omar SL, Wan Yusoff WNAB, Mohd Din MLB, Jamaludin NAB, Wan Taib WR, Esa E, Mohd Yasin N.
Aziz NA, et al. Among authors: abdul hamid fs.
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.
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