25 results on '"Qasem, Ebtesam"'
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2. Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer
3. Analysis of ALK, IDH1, IDH2 and MMP8 somatic mutations in differentiated thyroid cancers
4. A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population
5. GPCR-mediated PI3K pathway mutations in pediatric and adult thyroid cancer
6. Correction to: Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer
7. Familial paraganglioma due to a novel SDHB mutation: familial phenotypic heterogeneity and a potentially novel manifestation
8. Molecular genetics and phenotype/genotype correlation of 5-α reductase deficiency in a highly consanguineous population
9. Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer
10. Lung Metastasis in Pediatric Thyroid Cancer: Radiological Pattern, Molecular Genetics, Response to Therapy, and Outcome
11. Mutational analysis of rare subtypes of congenital adrenal hyperplasia in a highly inbred population
12. A high rate of novel CYP11B1 mutations in Saudi Arabia
13. Single Point Mutations in Pediatric Differentiated Thyroid Cancer
14. Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancer
15. HABP2 Gene Mutations Do Not Cause Familial or Sporadic Non-Medullary Thyroid Cancer in a Highly Inbred Middle Eastern Population
16. Uncommon TERT Promoter Mutations in Pediatric Thyroid Cancer
17. Absence of somatic mutations of the mTOR gene in differentiated thyroid cancer
18. Lung Metastasis in Pediatric Thyroid Cancer: Radiological Pattern, Molecular Genetics, Response to Therapy, and Outcome.
19. Absence of EIF1AX, PPM1D, and CHEK2mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer
20. TERT promoter mutations in thyroid cancer: a report from a Middle Eastern population
21. Divergent Gender Identity in Three Siblings With 46Xx Karyotype and Severely Virilizing Congenital Adrenal Hyperplasia Caused by A Novel Cyp11B1 Mutation
22. Apparent Mineralocorticoid Excess Caused by a Novel Mutation in 11-β Hydroxysteroid Dehydrogenase type 2 Enzyme: its Genetics and Response to Therapy
23. Case Report Abstracts
24. Correction to: Absence of EIF1AX, PPM1D, and CHEK2mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer
25. Familial paraganglioma due to a novel SDHBmutation: familial phenotypic heterogeneity and a potentially novel manifestation
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