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2019 | 2 |
2020 | 2 |
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Page 1
Human Oropharyngeal Candidiasis: From Etiology to Current Treatment.
Crit Rev Immunol. 2023;43(3):15-24. doi: 10.1615/CritRevImmunol.2023049730.
Crit Rev Immunol. 2023.
PMID: 37824374
Novel homozygous nonsense variant in MLPH causing Griscelli syndrome type 3 in a consanguineous Pakistani family.
Wasif N, Parveen A, Bashir H, Ashraf F, Ali E, Khan KR, Arif A.
Wasif N, et al. Among authors: bashir h.
J Dermatol. 2020 Nov;47(11):e382-e383. doi: 10.1111/1346-8138.15565. Epub 2020 Aug 30.
J Dermatol. 2020.
PMID: 32864751
No abstract available.
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A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family.
Khan SA, Khan MA, Muhammad N, Bashir H, Khan N, Muhammad N, Yilmaz R, Khan S, Wasif N.
Khan SA, et al. Among authors: bashir h.
BMC Med Genet. 2020 May 7;21(1):97. doi: 10.1186/s12881-020-01038-6.
BMC Med Genet. 2020.
PMID: 32380970
Free PMC article.
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A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations.
Parveen A, Mirza MU, Vanmeert M, Akhtar J, Bashir H, Khan S, Shehzad S, Froeyen M, Ahmed W, Ansar M, Wasif N.
Parveen A, et al. Among authors: bashir h.
Mol Genet Genomic Med. 2019 Sep;7(9):e902. doi: 10.1002/mgg3.902. Epub 2019 Jul 25.
Mol Genet Genomic Med. 2019.
PMID: 31347285
Free PMC article.
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Deleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations.
Parveen A, Khan SA, Mirza MU, Bashir H, Arshad F, Iqbal M, Ahmad W, Wahab A, Fiaz A, Naz S, Ashraf F, Mobeen T, Aziz S, Ahmed SS, Muhammad N, Hassib NF, Mostafa MI, Gaboon NE, Gul R, Khan S, Froeyen M, Shoaib M, Wasif N.
Parveen A, et al. Among authors: bashir h.
Int J Mol Sci. 2019 Oct 24;20(21):5282. doi: 10.3390/ijms20215282.
Int J Mol Sci. 2019.
PMID: 31652981
Free PMC article.
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