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الرسائل والأطروحات الجامعية
1
0
Investigation of an association between human leukocyte antigens and systemic lupus erythematosus among Omani patients
Al-Mawaliyah, Nawar Hamdan.
Sultan Qaboos University
2017
Investigation of an association between human leukocyte antigens and systemic lupus erythematosus among Omani patients
الرسائل والأطروحات الجامعية
0
0
Characterization of TL9 expression in B lymphocytes of Omani patients with systemic lupus erythematosus (SLE)
Al-Busaidi, Juma Zaid.
2012
Characterization of TL9 expression in B lymphocytes of Omani patients with systemic lupus erythematosus (SLE)
مقالات الدوريات
0
0
No more milk in milk-alkali syndrome : a case report.
Al-Musawi, Ali.
Oman Medical Specialty Board.
2012-09
No more milk in milk-alkali syndrome : a case report.
مقالات الدوريات
3
0
Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome.
Hennies, Hans Christian.
American Society of Human Genetics.
2004-07-28
Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome.
مقالات الدوريات
0
0
Refractory seizure in childhood : Dyke-Davidoff-Masson syndrome revisited.
Dutta, Abhijit.
Oman Medical Specialty Board.
2016-07
Refractory seizure in childhood : Dyke-Davidoff-Masson syndrome revisited.
مقالات الدوريات
4
0
Spectrum of MKS1 and MKS3 mutations in Meckel syndrome : a genotype-phenotype correlation. mutation in brief #960. online.
Khaddour, Rana.
Wiley-Liss, Inc.
2007-05-01
Spectrum of MKS1 and MKS3 mutations in Meckel syndrome : a genotype-phenotype correlation. mutation in brief #960. online.
مقالات الدوريات
6
0
Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, kindler syndrome.
Ashton, Gabrielle H. S.
Blackwell
2004-01-01
Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, kindler syndrome.
مقالات الدوريات
0
0
One in three : congenital bent bone disease and intermittent hyperthermia in three siblings with Stuve-Wiedemann syndrome.
Koul, Roshan.
College of Medicine, Sultan Qaboos University.
2013-05
One in three : congenital bent bone disease and intermittent hyperthermia in three siblings with Stuve-Wiedemann syndrome.
مقالات الدوريات
0
0
Pearson's Marrow-pancreas syndrome.
Al-Tamemi, Salem H.
College of Medicine, Sultan Qaboos University.
2009-08
Pearson's Marrow-pancreas syndrome.
مقالات الدوريات
4
0
Aberrant splicing is a common mutational mechanism in MKS1, a key player in Meckel-Gruber syndrome.
Frank, Valeska.
Wiley-Liss, Inc.
2007-07-01
Aberrant splicing is a common mutational mechanism in MKS1, a key player in Meckel-Gruber syndrome.
مقالات الدوريات
5
0
Aberrant splicing is a common mutational mechanism in MKS1, a key player in Meckel-Gruber syndrome.
Frank, Valeska.
Wiley-Liss, Inc.
2007-07-01
Aberrant splicing is a common mutational mechanism in MKS1, a key player in Meckel-Gruber syndrome.
مقالات الدوريات
0
0
Rapunzel syndrome.
Dhinakar, Manjula.
Oman Medical Specialty Board.
2010-10
Rapunzel syndrome.
الرسائل والأطروحات الجامعية
0
0
Polycystic ovarian syndrome in Oman: risk factor profile, oxidative stress and psychological burden
Sulaiman, Maha Abdul Hussain Jaffar
Sultan Qaboos University
2018
Polycystic ovarian syndrome in Oman: risk factor profile, oxidative stress and psychological burden
الرسائل والأطروحات الجامعية
0
0
Assessment of risk factors related to nutrition and dietary intake among Omani women with polycystic ovarian syndrome.
Al-Fazariyah, Maryam Abdullah Said.
Sultan Qaboos University
2014
Assessment of risk factors related to nutrition and dietary intake among Omani women with polycystic ovarian syndrome.
مقالات الدوريات
0
0
Evaluation of the role of postnatal ambroxol in the prevention and treatment of respiratory distress syndrome in preterm neonates.
Elsayed, Hesham F.
College of Medicine, Sultan Qaboos University.
2006-12
Evaluation of the role of postnatal ambroxol in the prevention and treatment of respiratory distress syndrome in preterm neonates.
مقالات الدوريات
0
0
Neuroleptic malignant syndrome associated with lithium toxicity.
Patil, Vaibhav.
Oman Medical Specialty Board.
2016-07
Neuroleptic malignant syndrome associated with lithium toxicity.
مقالات الدوريات
1
0
Burnout syndrome in pediatric practice.
Al-Youbi, Reem A.
Oman Medical Specialty Board.
2013-07
Burnout syndrome in pediatric practice.
مقالات الدوريات
0
0
Prevalence of metabolic syndrome in patients with schizophrenia referred to Farabi Hospital, Kermanshah, Iran.
Shakeri, Jalal.
Oman Medical Specialty Board.
2016-07
Prevalence of metabolic syndrome in patients with schizophrenia referred to Farabi Hospital, Kermanshah, Iran.
مقالات الدوريات
0
0
Stewart Treves syndrome : a case report.
Güleç, Ali.
Oman Medical Specialty Board.
2014-03
Stewart Treves syndrome : a case report.
مقالات الدوريات
0
0
Is coasting valuable in all patients with any cause of infertility?.
Madani, Tahereh.
Oman Medical Specialty Board.
2016-11
Is coasting valuable in all patients with any cause of infertility?.
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