37 results on '"Kaul, Haiba"'
Search Results
2. SLC4A11 mutations causative of congenital hereditary endothelial dystrophy (CHED) progressing to Harboyan syndrome in consanguineous Pakistani families
3. Correction: Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, Pakistan
4. Fine mapping of chromosome 9 locus associated with congenital cataract
5. In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma
6. Editing Glia, Glip and Gliz Genes of Aspergillus Fumigatus Using Crispr/Cas System Renders Fungus Incapable to Produce Gliotoxin
7. Epidemiology of Different Types of Cancer in District Dera Ghazi Khan, Pakistan
8. Determination of Serum Trace Elements (Zn, Cu, and Fe) in Pakistani Patients with Rheumatoid Arthritis
9. Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, Pakistan
10. Genetic Polymorphism and serum levels of Insulin like Growth Factor-1 (Igf-1) in patients of rheumatoid arthritis.
11. Frequency of Different Types of Endothelial Corneal Dystrophies by Age, Gender, and Visual Acuity in Punjab, Pakistan
12. Delineating Novel and Known Pathogenic Variants in TYR, OCA2 and HPS-1 Genes in Eight Oculocutaneous Albinism (OCA) Pakistani Families
13. Prevalence and Association of Different Levels of Intellectual Disability with Prenatal, Perinatal, Neonatal and Postnatal Factors
14. Association of Interleukin 10 (IL-10) Gene with Type 2 Diabetes Mellitus by Single Nucleotide Polymorphism of Its Promotor Region G/A 1082
15. Genetic mapping of autosomal recessive microspherophakia to chromosome 14q24.3 in a consanguineous Pakistani family and screening of exon 36 of LTBP2 gene
16. Ectopia Lentis in a Consanguineous Pakistani Family and a Novel Locus on Chromosome 8q
17. Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani family
18. Clinical profile and screening of exon 6 and 14 of ABCB4 gene in obstetric cholestasis patients at a tertiary care hospital in Rawalpindi, Pakistan.
19. Cytochrome 2C19 and paraoxonase-1 polymorphisms and clopidogrel resistance in ischemic heart disease patients
20. Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3′ splice acceptor site of intron 2
21. Mutations in TYR and OCA2 associated with oculocutaneous albinism in Pakistani families
22. Mapping of a novel locus associated with autosomal recessive congenital cataract to chromosome 8p
23. Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1
24. Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family
25. A new locus for autosomal recessive congenital cataract identified in a Pakistani family
26. Fine mapping of chromosome 9 locus associated with congenital cataract
27. In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma
28. Interleukin 6 Receptor (IL6-R) Gene Polymorphisms Underlie Susceptibility to Rheumatoid Arthritis
29. Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts
30. Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3′ splice acceptor site of intron 2.
31. Determination of Serum Trace Elements (Zn, Cu, and Fe) in Pakistani Patients with Rheumatoid Arthritis
32. Missense mutation in SLC4A11 in two Pakistani families affected with congenital hereditary endothelial dystrophy (CHED2)
33. In silico analysis of five missense mutations in <italic>CYP1B1</italic> gene in Pakistani families affected with primary congenital glaucoma.
34. Prevalence of stromal corneal dystrophies in Lahore.
35. Homozygosity mapping of a consanguineous Pakistani family affected with oculocutaneous albinism to Tyrosinase gene.
36. Novel SIL1 mutations in consanguineous Pakistani families mapping to chromosomes 5q31.
37. Localization of autosomal recessive congenital cataracts in consanguineous Pakistani families to a new locus on chromosome 1p.
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