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Theses and Dissertations
0
0
Screening for P2X7 gene functional polymorphims apparently healthy and rheumatoid arthritis Omani subjects
Al-Gheilaniyah, Afrah Mohammed Hamed
Sultan Qaboos University
2008
Screening for P2X7 gene functional polymorphims apparently healthy and rheumatoid arthritis Omani subjects
Journal articles
0
0
Association of e-cadherin (CDH1) gene polymorphisms and gastric cancer risk.
Al-Moundhri, Mansour S.
Baishideng Publishing.
2010-07
Association of e-cadherin (CDH1) gene polymorphisms and gastric cancer risk.
Journal articles
0
0
Recessive developmental delay, small stature, microcephaly and brain calcifications with locus on chromosome 2.
Rajab, Anna.
Elsevier B. V.
2009-02
Recessive developmental delay, small stature, microcephaly and brain calcifications with locus on chromosome 2.
Journal articles
3
0
Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26.
Bayoumi, Riad.
BMJ Publishing Group.
2001-06-01
Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26.
Journal articles
0
0
Cytogenetic studies of 1232 patients with different sexual development abnormalities from the Sultanate of Oman.
Al-Alawiyah, Intisar.
Elsevier.
2016-02
Cytogenetic studies of 1232 patients with different sexual development abnormalities from the Sultanate of Oman.
Journal articles
0
0
Quantitative and qualitative corneal endothelial morphology of Omani patients with pseudoexfoliation syndrome.
Wali, Upender K.
College of Medicine, Sultan Qaboos University.
2008-11
Quantitative and qualitative corneal endothelial morphology of Omani patients with pseudoexfoliation syndrome.
Journal articles
0
0
Draft genomes of amanita jacksonii, ceratocystis albifundus, fusarium circinatum, huntiella omanensis, leptographium procerum, rutstroemia sydowiana, and sclerotinia echinophila.
van der Nest, Magriet A.
International Mycological Association.
2014-12
Draft genomes of amanita jacksonii, ceratocystis albifundus, fusarium circinatum, huntiella omanensis, leptographium procerum, rutstroemia sydowiana, and sclerotinia echinophila.
Journal articles
0
0
Chronic myeloid leukaemia : a paradigm for malignancy or just a strange disease?
McCann, Shaun R.
College of Medicine, Sultan Qaboos University.
2012-11
Chronic myeloid leukaemia : a paradigm for malignancy or just a strange disease?
Journal articles
0
0
Developmental and degenerative features in a complicated spastic paraplegia.
Manzini, M. Chiara.
Wiley.
2010-04
Developmental and degenerative features in a complicated spastic paraplegia.
Journal articles
0
0
A rare case of pericentric inversion, Inv (21) (p12;q22) in repeated pregnancy loss : a case report.
Tayebi, Naeimeh.
Oman Medical Specialty Board.
2011-11
A rare case of pericentric inversion, Inv (21) (p12;q22) in repeated pregnancy loss : a case report.
Journal articles
0
0
Genetic polymorphism of cytochrome p450 (2C19) enzyme in Iranian Turkman ethnic group.
Tabari, Robabeh Ghiyas.
Oman Medical Specialty Board.
2013-07
Genetic polymorphism of cytochrome p450 (2C19) enzyme in Iranian Turkman ethnic group.
Journal articles
0
0
Clinical outcomes and counselling issues regarding partial trisomy of terminal Xp in a child with developmental delay.
Sheath, Karen L.
College of Medicine, Sultan Qaboos University.
2013-05
Clinical outcomes and counselling issues regarding partial trisomy of terminal Xp in a child with developmental delay.
Journal articles
0
0
Pallister-Killian mosaic syndrome in an Omani newborn : a case report and literature review.
Elsheikh, Afaf.
Oman Medical Specialty Board.
2019-05
Pallister-Killian mosaic syndrome in an Omani newborn : a case report and literature review.
Journal articles
0
0
Follicular dendritic cell sarcoma : cytogenetics and pathological findings.
Udayakumar, Achandira M.
College of Medicine, Sultan Qaboos University.
2015-08
Follicular dendritic cell sarcoma : cytogenetics and pathological findings.
Journal articles
0
0
Evaluation of FTO rs9939609 and MC4R rs17782313 polymorphisms as prognostic biomarkers of obesity : a population-based cross-sectional study.
Mozafarizadeh, Mina.
Oman Medical Speciality Board.
2019-01
Evaluation of FTO rs9939609 and MC4R rs17782313 polymorphisms as prognostic biomarkers of obesity : a population-based cross-sectional study.
Journal articles
0
0
The association of a rare variant of -93, -53 promoter gene polymorphisms of lipoprotein lipase gene with obesity and insulin resistance.
Prakash, Jai.
Oman Medical Specialty Board.
2018-09
The association of a rare variant of -93, -53 promoter gene polymorphisms of lipoprotein lipase gene with obesity and insulin resistance.
Journal articles
0
0
Promoter hypermethylation of Wnt/β-catenin signaling pathway inhibitor WIF-1 gene and its association with MTHFR C677T polymorphism in patients with colorectal cancer.
Jalilvand, Ahmad.
Oman Medical Specialty Board.
2020-05
Promoter hypermethylation of Wnt/β-catenin signaling pathway inhibitor WIF-1 gene and its association with MTHFR C677T polymorphism in patients with colorectal cancer.
Journal articles
0
0
Association of rs12487066, rs12044852, rs10735781, rs3135388, rs6897932, rs1321172, rs10492972, and rs9657904 polymorphisms with multiple sclerosis in Iranian population.
Razavian, Takavar.
Oman Medical Specialty Board.
2020-07
Association of rs12487066, rs12044852, rs10735781, rs3135388, rs6897932, rs1321172, rs10492972, and rs9657904 polymorphisms with multiple sclerosis in Iranian population.
Journal articles
0
0
The C-565T polymorphism (rs2422493) of the ATP-binding cassette transporter A1 gene contributes to the development and severity of coronary artery disease in an Iranian population.
Mahmoodi, Khalil.
Oman Medical Specialty Board.
2018-07
The C-565T polymorphism (rs2422493) of the ATP-binding cassette transporter A1 gene contributes to the development and severity of coronary artery disease in an Iranian population.
Journal articles
0
0
De Novo duplication of 7p21.1p22.2 in a child with autism spectrum disorder and craniofacial dysmorphism.
Udayakumar, Achandira M.
College of Medicine, Sultan Qaboos University.
2015-08
De Novo duplication of 7p21.1p22.2 in a child with autism spectrum disorder and craniofacial dysmorphism.
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Human chromosome abnormalities--Diagnosis--Oman
(3)
Polymerase chain reaction
(3)
Chromosome abnormalities--Oman--Case reports
(2)
Coronary artery disease
(2)
Genotype
(2)
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Chromosome abberations--Oman
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Chromosome polymorphism
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Chromosome Xp11.3 deletion
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Colorectal cancer
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CYP2C19 genetic polymorphism
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Cytogenetics--Oman--Case reports
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Diabetes mellitus--India
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DNA methylation
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FTO protein, Human
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Gene expression
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Genetic polymorphism
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Genetic polymorphisms
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Genomes--Oman
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GSPT2 protein, Human
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Inflammation
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Intellectual disability
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Interleukin-18
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Iran
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Iranian Turkman ethnic group
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Leukemia--Diagnosis
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Lipoprotein lipase
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MAGED1 protein, Human
(1)
Melanocortin-4 receptor
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Microarray analysis
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Miscarriage
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Multiple sclerosis
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Mushrooms--Genetics--Oman
(1)
Neoplasms
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Obesity
(1)
Obesity--India
(1)
Pallister-Killian mosiac syndrome
(1)
PCR-RFLP (Polymerase chain reaction–restriction…
(1)
Pericentric inversion of chromosome 21
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Philadelphia chromosome
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Polymorphism
(1)
Polymorphism, Restriction fragment length
(1)
Polymorphism, Single nucleotide
(1)
Protein kinases--Inhibitors
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Restriction fragment length
(1)
Sarcoma--Diagnosis--Oman--Case reports
(1)
X chromosome
(1)
Author
Udayakumar, Achandira M.
(2)
Al-Alawiyah, Intisar.
(1)
Al-Gheilaniyah, Afrah Mohammed Hamed
(1)
Al-Moundhri, Mansour S.
(1)
Al-Shehhiyah, Halima.
(1)
Bayoumi, Riad.
(1)
Elsheikh, Afaf.
(1)
Hoseini, Fatemeh.
(1)
Jalilvand, Ahmad.
(1)
Mahmoodi, Khalil.
(1)
Manzini, M. Chiara.
(1)
McCann, Shaun R.
(1)
Mozafarizadeh, Mina.
(1)
Prakash, Jai.
(1)
Rajab, Anna.
(1)
Razavian, Takavar.
(1)
Sheath, Karen L.
(1)
Tabari, Robabeh Ghiyas.
(1)
Tayebi, Naeimeh.
(1)
van der Nest, Magriet A.
(1)
Wali, Upender K.
(1)
Publisher
Oman Medical Specialty Board
(9)
College of Medicine Sultan Qaboos University
(5)
Baishideng Publishing
(1)
BMJ Publishing Group
(1)
Elsevier
(1)
Elsevier B V
(1)
International Mycological Association
(1)
Oman Medical Speciality Board
(1)
Sultan Qaboos University
(1)
Wiley
(1)
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