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Journal articles
0
0
Further clinical and molecular delineation of Xp11.22 deletion syndrome : a case report.
Al-Shehhiyah, Halima.
Oman Medical Specialty Board.
2019-09
Further clinical and molecular delineation of Xp11.22 deletion syndrome : a case report.
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
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.
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
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
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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(13)
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Journal articles
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Journal articles
(11)
Theses and Dissertations
(1)
Subject
Human chromosome abnormalities--Diagnosis--Oman
(3)
Chromosome abnormalities--Oman--Case reports
(2)
Autism spectrum disorders--Oman--Case reports
(1)
Chromosome 12, 12p trisomy
(1)
Chromosome abberations--Oman
(1)
Chromosome abnormalities--Oman
(1)
Chromosome polymorphism
(1)
Chromosome Xp11.3 deletion
(1)
Cytogenetic analysis--Oman
(1)
Cytogenetics--Oman--Case reports
(1)
Genetic polymorphisms
(1)
Genomes--Oman
(1)
GSPT2 protein, Human
(1)
Head--Abnormalities--Diagnosis--Oman--Case reports
(1)
Inflammation
(1)
Intellectual disability
(1)
Klinefelter's syndrome--Oman
(1)
Leukemia--Diagnosis
(1)
MAGED1 protein, Human
(1)
Medical genetics--Oman--Case reports
(1)
Microarray analysis
(1)
Miscarriage
(1)
Mushrooms--Genetics--Oman
(1)
Nervous system--Diseases--Oman
(1)
Pallister-Killian mosiac syndrome
(1)
Pericentric inversion of chromosome 21
(1)
Philadelphia chromosome
(1)
Protein kinases--Inhibitors
(1)
Sarcoma--Diagnosis--Oman--Case reports
(1)
Sex chromosome abnormalities--Oman
(1)
Trisomy
(1)
X chromosome
(1)
X chromosome--New Zealand
(1)
Author
Udayakumar, Achandira M.
(2)
Al-Alawiyah, Intisar.
(1)
Al-Gheilaniyah, Afrah Mohammed Hamed
(1)
Al-Shehhiyah, Halima.
(1)
Bayoumi, Riad.
(1)
Elsheikh, Afaf.
(1)
Manzini, M. Chiara.
(1)
McCann, Shaun R.
(1)
Rajab, Anna.
(1)
Sheath, Karen L.
(1)
Tayebi, Naeimeh.
(1)
van der Nest, Magriet A.
(1)
Publisher
College of Medicine Sultan Qaboos University
(4)
Oman Medical Specialty Board
(3)
BMJ Publishing Group
(1)
Elsevier
(1)
Elsevier B V
(1)
International Mycological Association
(1)
Sultan Qaboos University
(1)
Wiley
(1)
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