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Year | Number of Results |
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2023 | 3 |
2024 | 3 |
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Page 1
Mutation profiling in South African patients with Cornelia de Lange syndrome phenotype.
Mol Genet Genomic Med. 2024 Jan;12(1):e2342. doi: 10.1002/mgg3.2342.
Mol Genet Genomic Med. 2024.
PMID: 38284454
Free PMC article.
Identifying the genetic causes of developmental disorders and intellectual disability in Africa: a systematic literature review.
Baine-Savanhu F, Macaulay S, Louw N, Bollweg A, Flynn K, Molatoli M, Nevondwe P, Seymour H, Carstens N, Krause A, Lombard Z.
Baine-Savanhu F, et al. Among authors: nevondwe p.
Front Genet. 2023 May 10;14:1137922. doi: 10.3389/fgene.2023.1137922. eCollection 2023.
Front Genet. 2023.
PMID: 37234869
Free PMC article.
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Advancing intercontinental collaboration in human genetics: success story of the African and European Young Investigator Forum.
Alimohamed MZ, Mnika K, Adadey SM, Barbosa-Matos R, Avram E, Nevondwe P, Akurugu WA, Mupfururirwa W, de Miranda Cerqueira JX, Dore R, Săbău ID, Kalantari S, da Silva ARGF, Anzaku AA, Matimba A, Chauke PA, Johari M, Nembaware V, Mroczek M.
Alimohamed MZ, et al. Among authors: nevondwe p.
Eur J Hum Genet. 2024 Jan;32(1):3-5. doi: 10.1038/s41431-023-01487-6. Epub 2023 Oct 26.
Eur J Hum Genet. 2024.
PMID: 37880422
No abstract available.
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A feasible molecular diagnostic strategy for rare genetic disorders within resource-constrained environments.
Mudau MM, Seymour H, Nevondwe P, Kerr R, Spencer C, Feben C, Lombard Z, Honey E, Krause A, Carstens N.
Mudau MM, et al. Among authors: nevondwe p.
J Community Genet. 2024 Feb;15(1):39-48. doi: 10.1007/s12687-023-00674-8. Epub 2023 Oct 10.
J Community Genet. 2024.
PMID: 37815686
Free PMC article.
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