14 results on '"Weber, B.H.F."'
Search Results
2. Solid lipid nanoparticle-based vectors intended for the treatment of X-linked juvenile retinoschisis by gene therapy: In vivo approaches in Rs1h-deficient mouse model
3. Differential diagnosis of primary failure of eruption (PFE) with and without evidence of pathogenic mutations in the PTHR1 gene
4. Trinucleotide repeat expansion in SCA 17/TBP in white patients with Huntington's disease-like phenotype
5. Multiallelic copy number variation in the complement component 4A (C4A) gene is associated with late-stage age-related macular degeneration (AMD)
6. Identification of an oncostatin M receptor mutation associated with familial primary cutaneous amyloidosis.
7. EFEMP1 is not associated with sporadic early onset drusen.
8. cDNA cloning and genomic structure of a novel gene (C11orf9) localized to chromosome 11q12→q13.1 which encodes a highly conserved, potential membrane-associated protein.
9. cDNA cloning and genomic structure of a novel gene (C11orf9) localized to chromosome 11q12→q13.1 which encodes a highly conserved, potential membrane-associated protein.
10. Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies.
11. Recent Advances in the Molecular Genetics of Hereditary Retinal Dystrophies with Primary Involvement of the Macula.
12. Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk
13. X-linked juvenile retinoschisis (RS) maps between DXS987 and DXS443.
14. The role of Properdin in the development and progression of age-related macular degeneration.
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