22 results on '"Soufir, Nadem"'
Search Results
2. Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P gene
3. Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants
4. P16 UV mutations in human skin epithelial tumors
5. Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma
6. MC1R and PTCH Gene Polymorphism in French Patients with Basal Cell Carcinomas
7. Association Between Endothelin Receptor B Nonsynonymous Variants and Melanoma Risk
8. p53 Patches are Not Increased in Patients with Multiple Nonmelanoma Skin Cancers
9. Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations
10. Familial pancreatic adenocarcinoma: A retrospective analysis of germline genetic testing in a French multicentre cohort.
11. Pancreatic ductal adenocarcinoma in BRCA2 mutation carriers.
12. A Large French Case-Control Study Emphasizes the Role of Rare Mc1R Variants in Melanoma Risk.
13. Genotype/Phenotype Analyses for 53 Crohn's Disease Associated Genetic Polymorphisms.
14. A Prevalent Mutation with Founder Effect in Xeroderma Pigmentosum Group C from North Africa.
15. Inhibition of the Proprotein Convertases Represses the Invasiveness of Human Primary Melanoma Cells with Altered p53, CDKN2A and N-Ras Genes.
16. Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma.
17. Association between INK4a-ARF and p53 mutations in skin carcinomas of xeroderma pigmentosum patients.
18. Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France.
19. Telomerase reverse transcriptase promoter mutations in primary cutaneous melanoma.
20. A Large French Case-Control Study Emphasizes the Role of Rare Mc1R Variants in Melanoma Risk.
21. M1291 Familial Pancreatic Cancer: BRCA2, CDKN2A and CDk 4 Gene Alterations and Screening of Relatives.
22. Prenatal manifestation in a family affected by nevoid basal cell carcinoma syndrome
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