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عدد العناصر المسترجعة: 9
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مقالات الدوريات
0
0
Cleidocranial dysplasia : a rare cause of disproportionate severe short stature.
Bhat, Manzoor.
Oman Medical Specialty Board.
2012-09
Cleidocranial dysplasia : a rare cause of disproportionate severe short stature.
مقالات الدوريات
2
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.
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.
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
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.
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مقالات الدوريات
مسح الجميع
النص الكامل فقط
اللغة
الأنجليزية
(9)
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مقالات الدوريات
(9)
تاريخ النشر
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مقالات الدوريات
(9)
الرسائل والأطروحات
(3)
الموضوع
Gene expression
(4)
17--hydroxysteriod dehydrogenase Type 3 deficiency
(1)
Acute myeloid leukemia
(1)
Ambiguous genitalia
(1)
Biomarkers
(1)
Charcot-Marie-tooth disease, Type 4B1
(1)
Cleidocranial dysplasia
(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)
Polymerase chain reaction
(1)
Polymorphism, Restriction fragment length
(1)
Prognosis
(1)
Schwannoma
(1)
Short stature
(1)
Skeletal dysplasia
(1)
SLC6A4 protein, Human
(1)
Tandem duplication
(1)
Testosterone
(1)
المؤلف
Al-Mawaliyah, Adhra.
(1)
Al-Sinaniyah, Aisha.
(1)
Bhat, Manzoor.
(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
(8)
College of Medicine Sultan Qaboos University
(1)
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