تجاوز إلى المحتوى الرئيسي
Toggle menu
تصفح ب
المؤلفين
المجموعات
الموضوعات
تواصل معنا
أدوات
ملاحظات الإصدار
تسليم محتوى
A-
A
A+
English
العربية
تسجيل الدخول
تسجيل الدخول
البحث الصوتي
×
ابدأ
توقف
Loading ...
Fulltext search
Media uses External URI
Sort by
Relevance
Views
العنوان
المؤلف
تاريخ النشر
Order
Asc
Desc
Results per page
20
40
60
80
البحث المتقدم
عدد العناصر المسترجعة: 11
تحديد الكل
أدوات البحث
تصدير بصيغة CSV
حفظ البحث
Items per page
20
40
60
80
Sort Options
الصلة
المشاهدات
العنوان
المؤلف
تاريخ النشر
Sort Order
ASC
DESC
شبكة
قائمة
تحديد الكل
مقالات الدوريات
0
0
Occurrence of optic neuritis and cervical cord schwannoma with Charcot-Marie-tooth Type 4B1disease.
Scott, Patrick.
Oman Medical Specialty Board.
2016-05
Occurrence of optic neuritis and cervical cord schwannoma with Charcot-Marie-tooth Type 4B1disease.
مقالات الدوريات
1
0
Implications of a Chr7q21.11 microdeletion and the role of the PCLO gene in developmental delay.
Mazzaschi, Roberto L.
College of Medicine, Sultan Qaboos University.
2013-05
Implications of a Chr7q21.11 microdeletion and the role of the PCLO gene in developmental delay.
مقالات الدوريات
0
0
Detection of CTX-M-15 among uropathogenic escherichia coli isolated from five major hospitals in Tripoli, Libya.
Zorgani, Abdulaziz.
Oman Medical Specialty Board.
2017-07
Detection of CTX-M-15 among uropathogenic escherichia coli isolated from five major hospitals in Tripoli, Libya.
الرسائل والأطروحات الجامعية
0
0
Developing Gene Therapy for Duchenne muscular dystrophy using Adeno Associated virus (AAV) Expressing Estrogen Related Receptor Gamma (ERRγ)
ALSiyabi, Muzna
Muzna ALSiyabi
2018
Developing Gene Therapy for Duchenne muscular dystrophy using Adeno Associated virus (AAV) Expressing Estrogen Related Receptor Gamma (ERRγ)
مقالات الدوريات
0
0
Genetic biomarkers in association with depressive disorder in UAE residents : a pilot case study.
Mahmood, Nailah.
Oman Medical Specialty Board.
2021-07
Genetic biomarkers in association with depressive disorder in UAE residents : a pilot case study.
مقالات الدوريات
0
0
Characteristics and prognosis of adult acute myeloid leukemia with internal tandem duplication in the FLT3 gene.
Al-Mawaliyah, Adhra.
Oman Medical Specialty Board.
2013-11
Characteristics and prognosis of adult acute myeloid leukemia with internal tandem duplication in the FLT3 gene.
الرسائل والأطروحات الجامعية
0
0
Apolipoprotein E gene polymorphism with ischemic stroke in Omani patients : a hospital-based case-control study
Gharbal, Ali Husain.
Sultan Qaboos University
2016
Apolipoprotein E gene polymorphism with ischemic stroke in Omani patients : a hospital-based case-control study
الرسائل والأطروحات الجامعية
0
0
Agrobacterium Mediated Transformation of cry1C Gene into Omani Tobacco Cultivar
Al-Maamariyah, Alghalyia Humaid Khamis.
Sultan Qaboos University
2007
Agrobacterium Mediated Transformation of cry1C Gene into Omani Tobacco Cultivar
مقالات الدوريات
0
0
The expression of activating receptor gene of natural killer cells (KLRC3) in patients with Type 1 diabetes mellitus (T1DM).
Shalaby, Dalia.
Oman Medical Specialty Board.
2017-07
The expression of activating receptor gene of natural killer cells (KLRC3) in patients with Type 1 diabetes mellitus (T1DM).
مقالات الدوريات
0
0
Evaluation of the role of -137G/C single nucleotide polymorphism (rs187238) and gene expression levels of the IL-18 in patients with coronary artery disease.
Hoseini, Fatemeh.
Oman Medical Specialty Board.
2018-03
Evaluation of the role of -137G/C single nucleotide polymorphism (rs187238) and gene expression levels of the IL-18 in patients with coronary artery disease.
مقالات الدوريات
0
0
A novel mutation causing 17-β-hydroxysteroid dehydrogenase Type 3 deficiency in an Omani child : first case report and review of literature.
Al-Sinaniyah, Aisha.
Oman Medical Specialty Board.
2015-03
A novel mutation causing 17-β-hydroxysteroid dehydrogenase Type 3 deficiency in an Omani child : first case report and review of literature.
التصفية
x
النص الكامل فقط
اللغة
الأنجليزية
(11)
الفئة
مقالات الدوريات
(8)
الرسائل والأطروحات الجامعية
(3)
تاريخ النشر
المجموعة
مقالات الدوريات
(8)
الرسائل والأطروحات
(3)
الموضوع
Gene expression
(4)
17--hydroxysteriod dehydrogenase Type 3 deficiency
(1)
Acute myeloid leukemia
(1)
Agrobacterium
(1)
Ambiguous genitalia
(1)
Apolipoprotein E gene.
(1)
Apolipoproteins
(1)
Biomarkers
(1)
Brain Ischemia
(1)
Cerebrovascular disease
(1)
Charcot-Marie-tooth disease, Type 4B1
(1)
Coronary artery disease
(1)
CTX-M-15 gene
(1)
Delta 4-androstenedione
(1)
Depressive disorder
(1)
Developmental disabilities--Diagnosis
(1)
Diabetes mellitus, Type 1
(1)
Disorder of sex development, 46,XY
(1)
E. coli
(1)
ESBL
(1)
Estrone
(1)
FLT3 gene
(1)
HSD17B3 gene
(1)
Interleukin-18
(1)
Killer cells, Natural
(1)
KLRC3 protein, Human
(1)
Libya
(1)
M1
(1)
MTMR2 gene
(1)
Mutation
(1)
Optic neuritis
(1)
Plant gene isolation
(1)
Plant genetic transformation
(1)
Polymerase chain reaction
(1)
Polymorphism, Restriction fragment length
(1)
Prognosis
(1)
Schwannoma
(1)
Skeletal muscle^ gene therapy^ AAV virus^ ERRγ
(1)
SLC6A4 protein, Human
(1)
Stroke
(1)
Tandem duplication
(1)
Testosterone
(1)
tobacco
(1)
Transgenic plants
(1)
المؤلف
Al-Maamariyah, Alghalyia Humaid Khamis.
(1)
Al-Mawaliyah, Adhra.
(1)
Al-Sinaniyah, Aisha.
(1)
ALSiyabi, Muzna
(1)
Gharbal, Ali Husain.
(1)
Hoseini, Fatemeh.
(1)
Mahmood, Nailah.
(1)
Mazzaschi, Roberto L.
(1)
Scott, Patrick.
(1)
Shalaby, Dalia.
(1)
Zorgani, Abdulaziz.
(1)
الناشر
Oman Medical Specialty Board
(7)
Sultan Qaboos University
(2)
College of Medicine Sultan Qaboos University
(1)
Muzna ALSiyabi
(1)
sfy39587stp18