Found: 15
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Serum and salivary Cu/Zn ratio as a diagnostic biomarker for oral submucosal fibrosis: an analysis of trace metals and LOX gene variants.
- Published in:
- BioMetals, 2024, v. 37, n. 2, p. 447, doi. 10.1007/s10534-023-00561-2
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- Article
Association of methylenetetrahydrofolate reductase gene variant C677T and folate levels in non-syndromic cleft lip/palate among Sindhi, Pakistani population.
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- Journal of the Pakistan Medical Association, 2024, v. 74, n. 1, p. 145, doi. 10.47391/JPMA.9273
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- Article
Relationship between aging and control of metabolic syndrome with telomere shortening: a cross-sectional study.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-44715-1
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- Article
Spectrum of HBB gene variants and major endocrine complications in thalassemia patients of Pakistan.
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- Journal of the Pakistan Medical Association, 2023, v. 73, n. 10, p. 2013, doi. 10.47391/JPMA.8599
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- Article
Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani Pedigrees.
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- Genes, 2023, v. 14, n. 2, p. 404, doi. 10.3390/genes14020404
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- Article
Genetic Counselling and Genetic Diseases.
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- Journal of Liaquat University of Medical & Health Sciences, 2022, v. 21, n. 4, p. 236, doi. 10.22442/jlumhs.2022.01011
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- Article
Disease-associated variants of Gap Junction Beta 2 protein (GJB2) in the deaf population of Southern Punjab of Pakistan.
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- PLoS ONE, 2021, v. 16, n. 10, p. 1, doi. 10.1371/journal.pone.0259083
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- Article
Biallelic Variants in EPHA2 Identified in Three Large Inbred Families with Early-Onset Cataract.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 19, p. 10655, doi. 10.3390/ijms221910655
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- Article
P.arg102ser is a common Pde6a mutation causing autosomal recessive retinitis pigmentosa in Pakistani families.
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- Journal of the Pakistan Medical Association, 2021, v. 71, n. 3, p. 816, doi. 10.47391/JPMA.256
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- Article
MTHFR and F5 genetic variations have association with preeclampsia in Pakistani patients: a case control study.
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- BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0905-9
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- Article
Consanguinity: A blessing or menace at population level?
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- Annals of Human Genetics, 2019, v. 83, n. 4, p. 214, doi. 10.1111/ahg.12308
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- Article
SE33 locus as a reliable genetic marker for forensic DNA analysis systems.
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- Turkish Journal of Medical Sciences, 2018, v. 48, n. 3, p. 611, doi. 10.3906/sag-1801-21
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- Article
IL28B rs12980275 polymorphism shows association with response to treatment in Pakistani patients with Chronic Hepatitis C.
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- Journal of Medical Virology, 2015, v. 87, n. 5, p. 814, doi. 10.1002/jmv.24100
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- Article
Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.
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- Human Molecular Genetics, 2013, v. 22, n. 10, p. 1960, doi. 10.1093/hmg/ddt043
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- Article
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing.
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- Human Mutation, 2007, v. 28, n. 10, p. 1014, doi. 10.1002/humu.20556
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- Article