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You searched for: Author/Creator Amr, Khalda

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2. Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development. Issue 6 (19th March 2021)

3. Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype–phenotype correlations. Issue 6 (23rd April 2013)

4. Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations. (18th August 2015)

7. Expanding the phenome and variome of skeletal dysplasia. (December 2018)

9. IL-6 −174G/C polymorphism in obese adolescents with nonalcoholic fatty liver disease and its relation to metabolic and biochemical markers. Issue 1 (January 2016)

10. Impact of type 2 diabetes mellitus on the immunoregulatory characteristics of adipose tissue-derived mesenchymal stem cells. (November 2021)