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Journal articles
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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.
Journal articles
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.
Journal articles
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.
Journal articles
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.
Journal articles
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.
Journal articles
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.
Journal articles
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).
Journal articles
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.
Journal articles
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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Gene expression
(4)
17--hydroxysteriod dehydrogenase Type 3 deficiency
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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
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Mutation
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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)
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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)
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Oman Medical Specialty Board
(8)
College of Medicine Sultan Qaboos University
(1)
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