15 results on '"Temtamy, Samia"'
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2. Cytoskeleton and nuclear lamina affection in recessive osteogenesis imperfecta: A functional proteomics perspective
3. Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study
4. Chapter 19 - BMP1 Mutations in Autosomal Recessive Osteogenesis Imperfecta
5. Chapter 18 - OSX/SP7 Mutations and Osteogenesis Imperfecta
6. List of Contributors
7. A postaxial polydactyly-dental-vertebral syndrome
8. Macrodactyly, hemihypertrophy, and connective tissue nevi: Report of a new syndrome and review of the literature
9. The Coffin-Lowry syndrome: An inherited faciodigital mental retardation syndrome
10. Extending the scope of the VATER association: Definition of the VATER syndrome
11. Medical genetics 1962
12. Medical genetics 1963
13. The syndrome of aplasia cutis congenita with terminal, transverse defects of limbs
14. On the nomenclature of a “new” syndrome
15. On anomalies associated with radial dysplasia
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