Gene mutation in relation to thyroid hormone

Mutation analysis of steroid 21 hydroxylase gene in a group of Egyptian children with congenital adrenal hyperplasia

Etiology of congenital hypothyroidism revealed by newborn screening

The clinical significance of thyroglobulin and thyroid peroxidase autoantibodies in type 1 diabetic patients and their relatives

Molecular characterization of 21 hydroxylase deficiency of congenital adrenal hyperplasia in Egyptian children

Vitamin D receptor gene polymorphism in type 1 diabetes mellitus

The clinical significance of thyroglobulin and thyroid peroxidase autoantibodies in type 1 diabetic patients and their relatives

Paraoxonase gene polymorphism as a marker for early microvascular complications in type 1 diabetes mellitus

Congenital anomalies associated with congenital hypothyroidism

Serum insulin-like growth factor-I (IGF-I) and its binding protein-3 in thyroid disorders