Biomedicine Congress - Biology Congress - Medicine Congress

Mehri Khatami

Yazd University
yazd, iran

Abstracts, Mehri Khatami [Author]

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• Identification of Heterozygote Mutations in Exon 1 of NKX2.1 Gene in Patients with Congenital Hypothyroidism

  Metabolism and Metabolic Diseases

  Introduction: Congenital hypothyroidism (CH) is a most common congenital endocrine disorder, affecting 1 in 3000 to 4000...Read more

• A Novel Missense Mutation (G106R) in Thyroid Stimulating Hormone β-subunit gene in Patients with Central Congenital Hypothyroidism

  Metabolism and Metabolic Diseases

  Background: Central Congenital hypothyroidism (CCH) is a rare and evades diagnosis on thyroid stimulating hormone (TSH)-...Read more

• Novel and Heteroplasmic Mutations in Mitochondrial Coding Genes in Iranian Patients with Familial Adenomatous Polyposis (FAP)

  Medical Genetics

  Familial Adenomatous Polyposis (FAP) is an Autosomal dominant inherited disorder and a rare form‌ of colorectal cance...Read more