Skip to main content
Toggle menu
Browse By
Authors
Collections
Subjects
Contact Us
Tools
Release notes
Submit content
A-
A
A+
English
العربية
Log in
Log in
Voice search
×
Start
Stop
Loading ...
Fulltext search
Media uses External URI
Sort by
Relevance
Views
Title
Author
Date Issued
Order
Asc
Desc
Items per page
20
40
60
80
Advanced Search
2 results found
Genetics
Select all
Search tools
Export to CSV
Save search
Items per page
20
40
60
80
Sort Options
Relevance
Views
Title
Author
Date Issued
Sort Order
ASC
DESC
Grid
List
Select all
Journal articles
1
0
A novel deletion mutation of exon 2 of the C19orf12 gene in an Omani family with mitochondrial membrane protein-associated neurodegeneration (MPAN).
Al-Macki, Nabil.
Oman Medical Specialty Board.
2017-01
A novel deletion mutation of exon 2 of the C19orf12 gene in an Omani family with mitochondrial membrane protein-associated neurodegeneration (MPAN).
Theses and Dissertations
1
0
Diversity of tetracycline resistant genes of Escherichia coli from environmental samples in Oman
Al-Sharjyah, Nawal Khalfan.
Sultan Qaboos University
2013
Diversity of tetracycline resistant genes of Escherichia coli from environmental samples in Oman
Filters
x
Genetics
Clear All
Fulltext only
Language
English
(2)
Category
Journal articles
(1)
Theses and Dissertations
(1)
Publication Date
Collection
Journal articles
(1)
Theses and Dissertations
(1)
Subject
(-)
Genetics
(2)
Beta lactamases
(7)
Human engineering
(4)
AIDS (Disease)
(3)
Beta lactam antibiotics
(3)
Beta lactamases--Oman
(3)
Diabetes
(3)
Drug resistance in microorganisms
(3)
Human chromosome abnormalities--Diagnosis--Oman
(3)
Human genetics--Oman
(3)
Human genetics--Variation--Oman
(3)
Anti-infective Agents
(2)
Carbohydrates in human nutrition
(2)
Convenience foods
(2)
Food
(2)
Fruit in human nutrition--Arab countries
(2)
Gene expression
(2)
Glycemic index
(2)
Human cell culture
(2)
human resources
(2)
Magnetic Resonance Imaging
(2)
Proteins in human nutrition
(2)
Vegetables in human nutrition--Arab countries
(2)
Work environment
(2)
Autosomal recessive Parkinsonism
(1)
Bacteria
(1)
Chromosome Xp11.3 deletion
(1)
Codon, Nonsense
(1)
Codon, Terminator
(1)
Cystic fibrosis
(1)
Date palm
(1)
Diabetes mellitus, Type 1
(1)
Drug resistance
(1)
Genetic polymorphism
(1)
Genotype
(1)
GSPT2 protein, Human
(1)
Infant, Newborn
(1)
Intellectual disability
(1)
Ki-67 antigen
(1)
Killer cells, Natural
(1)
KLRC3 protein, Human
(1)
MAGED1 protein, Human
(1)
Meningitis
(1)
Microarray analysis
(1)
Mutation
(1)
Ovarian neoplasms
(1)
PARK 2 protein, Human
(1)
Parkinson's disease
(1)
Phenotype
(1)
Ultrasound imaging
(1)
Author
Al-Macki, Nabil.
(1)
Al-Sharjyah, Nawal Khalfan.
(1)
Publisher
Oman Medical Specialty Board
(1)
Sultan Qaboos University
(1)
sfy39587stp18