• HSD17B3 gene
• مسح الجميع

• النص الكامل فقط

اللغة

• الأنجليزية (1)

الفئة

• مقالات الدوريات (1)

المجموعة

• مقالات الدوريات (1)

الموضوع

• (-) HSD17B3 gene (1)
• Attention-deficit hyperactivity disorder--Oman (2)
• Autism in children (2)
• Autistic Disorder (2)
• Autologous transplantation (2)
• Lymphoma (2)
• Lymphoproliferative disorder (2)
• Multiple myeloma (2)
• Stem cell (2)
• 17--hydroxysteriod dehydrogenase Type 3 deficiency (1)
• Ambiguous genitalia (1)
• Antioxidants (1)
• Attention deficit disorder with hyperactivity (1)
• Attention deficit hyperactivity disorder--Oman (1)
• Autism spectrum (1)
• Autism spectrum disorder (1)
• Autosomal recessive disorder (1)
• Benzodiazepine (1)
• Biomarkers (1)
• Catatonia (1)
• Chest pain (1)
• Children--Health and hygiene (1)
• Congenital diarrheal disorder (1)
• Coronary artery disease (1)
• Delta 4-androstenedione (1)
• Demographic factors--Oman (1)
• Depressive disorder (1)
• Disorder of sex development, 46,XY (1)
• Distress (1)
• Estrone (1)
• Gene expression (1)
• Genetics (1)
• Hereditary neuropathy (1)
• Intestinal transplantation (1)
• Microvillous inclusion disease (1)
• Mood disorder (1)
• Nerve conduction (1)
• Neuro muscular disorder (1)
• Peripheral nervous system (1)
• Prevalence (1)
• Primary Health Care--Oman (1)
• Quality of life (1)
• Risk factors--Oman (1)
• Sanjad Sakati syndrome (1)
• SLC6A4 protein, Human (1)
• Small intestine biopsy (1)
• Smoking (1)
• Somatoform disorder (1)
• Testosterone (1)
• Tuberous sclerosis--Oman--Case reports (1)

المؤلف

• Al-Sinaniyah, Aisha. (1)

الناشر

• Oman Medical Specialty Board (1)