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مقالات الدوريات
0
0
Should we look for celiac disease in irritable bowel syndrome?.
Amiriani, Taghi.
Oman Medical Specialty Board.
2011-01
Should we look for celiac disease in irritable bowel syndrome?.
مقالات الدوريات
0
0
Vitamin D deficiency in patients with irritable Bowen syndrome : does it exist?.
Khayyat, Yasir.
Oman Medical Specialty Board.
2015-03
Vitamin D deficiency in patients with irritable Bowen syndrome : does it exist?.
مقالات الدوريات
0
0
How predictive are the signs and symptoms of small bowel obstruction.
Al-Salamah, Saleh Mohammad.
Oman Medical Specialty Board.
2012-07
How predictive are the signs and symptoms of small bowel obstruction.
مقالات الدوريات
3
0
Incidence, prevalence, and clinical epidemiology of inflammatory bowel disease in the Arab world : a systematic review and meta-analysis.
Mosli, Mahmoud.
S. Karger AG.
2021-09-01
Incidence, prevalence, and clinical epidemiology of inflammatory bowel disease in the Arab world : a systematic review and meta-analysis.
مقالات الدوريات
0
0
An unusual cause of gastrointestinal obstruction : bezoar.
Abbas, Tariq O.
Oman Medical Specialty Board.
2011-03
An unusual cause of gastrointestinal obstruction : bezoar.
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.
الرسائل والأطروحات الجامعية
0
0
Identification of cellular targets in regulating inflammatory pathways
Al-Araimiyah, .Amna Salim
Sultan Qaboos University
2017
Identification of cellular targets in regulating inflammatory pathways
مقالات الدوريات
0
0
Pediatric Crohn's disease in Bahrain.
Isa, Hasan M.
Oman Medical Specialty Board.
2018-07
Pediatric Crohn's disease in Bahrain.
مقالات الدوريات
0
0
Signet ring cell lymphoma of the small bowel : a case report.
Basir, Norwani.
Oman Medical Specialty Board.
2012-11
Signet ring cell lymphoma of the small bowel : a case report.
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.
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