• النص الكامل فقط

اللغة

• الأنجليزية (11)

الفئة

• مقالات الدوريات (10)
• الرسائل والأطروحات الجامعية (1)

تاريخ النشر

المجموعة

• مقالات الدوريات (10)
• الرسائل والأطروحات (1)

الموضوع

• Mutation (8)
• Genes (2)
• Genetic testing (2)
• Acrodermatitis enteropathica (1)
• Adrenal gland neoplasms (1)
• Alkaline phosphatase (1)
• Ataxia telangiectasia (1)
• Autosomal dominant hypercholesterolemia (1)
• Beta thalassemia major (1)
• CFTR protein, Human (1)
• Charcot-Marie-tooth disease, Type 4B1 (1)
• Chromogranin A (1)
• Cystic fibrosis (1)
• Cystic fibrosis transmembrane conductance… (1)
• Diabetes mellitus (1)
• Dystonia (1)
• Family characteristics--Oman (1)
• Ferritin (1)
• Gamma-aminobutyric acid (1)
• Genetic disorders (1)
• Germ-line mutation (1)
• Hemosiderosis (1)
• HFE mutation (1)
• Hyperchlosterolaemia (1)
• Hyperglycemia (1)
• Infant, Newborn (1)
• Infants (1)
• Insulin (1)
• Magnetic Resonance Imaging (1)
• MTMR2 gene (1)
• Mutation (Biology) (1)
• Optic neuritis (1)
• Paraganglioma (1)
• PCSK9 protien (1)
• Phenotype (1)
• Receptors, GABA (1)
• Receptors, Thyroid hormone (1)
• Renal pheochromocytoma (1)
• Schwannoma (1)
• Thyroid hormone resistance syndrome (1)
• Whole exome sequencing (1)
• Zinc (1)

المؤلف

• Al-Balushi, Said. (1)
• Al-Waili, Khalid. (1)
• Al-Zidiyah, Ward Al-Muna Ali Rashid. (1)
• Al Naamaniyah, Asma. (1)
• Al Shidhaniyah, Azza. (1)
• Khair, Abdulhafeez M. (1)
• Pambinezhthu, Fathima. (1)
• Scott, Patrick. (1)
• Soltanpour, Mohammad Soleiman. (1)
• Yahaya, Tajudeen O. (1)
• Zaki-Dizaji, Majid. (1)

الناشر

• Oman Medical Specialty Board (10)
• Sultan Qaboos University (1)