41 results on '"Ayadi, Hammadi"'
Search Results
2. DFNB66 and DFNB67 loci are non allelic and rarely contribute to autosomal recessive nonsyndromic hearing loss
3. A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family
4. No major genes in autoimmune thyroid diseases: complex segregation and epidemiological studies in a large Tunisian pedigree
5. A potential role of TNFR gene polymorphisms in autoimmune thyroid diseases in the Tunisian population
6. A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1
7. Allelic structure and distribution of 103 STR loci in a Southern Tunisian population
8. Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian Population
9. Proteomic approaches for discovering biomarkers of diabetic nephropathy
10. Genetic variants in RELN are associated with otosclerosis in a non-European population from Tunisia
11. Gene and protein markers of diabetic nephropathy
12. The A/T mutation in exon 2 of the DNASE1 gene is not present in Tunisian patients with systemic lupus erythematosus or in healthy subjects
13. PDS Is a New Susceptibility Gene to Autoimmune Thyroid Diseases: Association and Linkage Study
14. Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin
15. Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE
16. Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates
17. SLC26A4 Variations Among Graves’ Hyper-Functioning Thyroid Gland
18. A 20year history of clinical and genetic study of thyroid autoimmunity in a Tunisian multigenerational family: Evidence for gene interaction
19. Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis.
20. Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations
21. Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059_1066insC mutation of the PRSS56 gene
22. Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases
23. Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family
24. Re-assigning the DFNB33 locus to chromosome 10p11.23–q21.1
25. Aspects cliniques et biologiques de l’azoospermie chez l’homme infertile en Tunisie
26. Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1
27. Cloning and Characterization of SLC26A6, a Novel Member of the Solute Carrier 26 Gene Family
28. Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates
29. A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23–24.2
30. Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.
31. Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene.
32. A Newly Identified Locus for Usher Syndrome Type I, USH1E, Maps to Chromosome 21q21.
33. Cloning and Characterization of SLC26A6,a Novel Member of the Solute Carrier 26 Gene Family
34. Re-assigning the DFNB33 locus to chromosome 10p11.23–q21.1.
35. Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059-1066insC mutation of the PRSS56 gene.
36. A 20 year history of clinical and genetic study of thyroid autoimmunity in a Tunisian multigenerational family: Evidence for gene interaction.
37. Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness.
38. Identification of candidate regions for a novel Usher syndrome type II locus.
39. Tag STS in the AZF region associated with azoospermia in a Tunisian population.
40. Contribution of immunological and genetic investigations to improve classification of patients with congenital muscular dystrophy.
41. PDS is a new susceptibility gene to autoimmune thyroid diseases: association and linkage study.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.