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مقالات الدوريات
0
0
A case report of basal ganglia calcification : a rare finding of hypoparathyroidism.
Basak, Ramen C.
Oman Medical Specialty Board.
2009-07
A case report of basal ganglia calcification : a rare finding of hypoparathyroidism.
مقالات الدوريات
0
0
Congenital anomalies in infant with congenital hypothyroidism.
Razavi, Zahra.
Oman Medical Specialty Board.
2012-09
Congenital anomalies in infant with congenital hypothyroidism.
الرسائل والأطروحات الجامعية
0
0
Assessment of folate and vitamin B12 status among newly diagnosed Omani autistic children
Al-Khalili, Maha Ali Abdullah.
Sultan Qaboos University
2012
Assessment of folate and vitamin B12 status among newly diagnosed Omani autistic children
مقالات الدوريات
0
0
Neonatal stridor in familial congenital laryngeal paralysis (Plott syndrome) : a case study in an Omani family.
Shatla, Emad Sadek.
Oman Medical Specialty Board.
2017-11
Neonatal stridor in familial congenital laryngeal paralysis (Plott syndrome) : a case study in an Omani family.
مقالات الدوريات
0
0
Familial ectrodactyly syndrome in a Nigerian child : a case report.
Durowaye, Mathew.
Oman Medical Specialty Board.
2011-07
Familial ectrodactyly syndrome in a Nigerian child : a case report.
مقالات الدوريات
3
0
Genetic analysis and outcomes of Omani children with steroid-resistant nephrotic syndrome.
Al-Riyami, Mohamed S.
John Wiley and Sons Inc.
2023-09-01
Genetic analysis and outcomes of Omani children with steroid-resistant nephrotic syndrome.
الرسائل والأطروحات الجامعية
0
0
Mutation analysis of KI13B as a candidate gene for autosomal recessive hereditary spastic paraplegia.
Al-Barwaniyah, Hamida Sarhan.
Sultan Qaboos University
2006
Mutation analysis of KI13B as a candidate gene for autosomal recessive hereditary spastic paraplegia.
مقالات الدوريات
0
0
Berardinelli-Seip syndrome and essential thrombocytosis : an unusual association.
Alzu'bi, Ali A.
Oman Medical Specialty Board.
2020-05
Berardinelli-Seip syndrome and essential thrombocytosis : an unusual association.
مقالات الدوريات
0
0
Scapular bronchogenic cyst : a case report and literature review.
Al-Balushiyah, Zainab.
Oman Medical Specialty Board.
2012-03
Scapular bronchogenic cyst : a case report and literature review.
مقالات الدوريات
0
0
Adolescents and adults with congenital heart diseases in Oman.
Al-Balushi, Asim.
Oman Medical Specialty Board.
2015-01
Adolescents and adults with congenital heart diseases in Oman.
مقالات الدوريات
0
0
Fetal amelia : a case report.
Al-Riyamiyah, Nihal.
Oman Medical Specialty Board.
2012-01
Fetal amelia : a case report.
مقالات الدوريات
0
0
Patent contralateral processus vaginalis in infants and children : Is herniotomy justified?.
Zakaria, Ossama M.
Oman Medical Specialty Board.
2018-11
Patent contralateral processus vaginalis in infants and children : Is herniotomy justified?.
مقالات الدوريات
0
0
Coarctation of the aorta, known yet can be missed.
Al-Balushi, Asim.
Oman Medical Specialty Board.
2013-05
Coarctation of the aorta, known yet can be missed.
مقالات الدوريات
0
0
The prevalence of congenital malformations and its correlation with consanguineous marriages.
Tayebi, Naeimeh.
Oman Medical Specialty Board.
2010-01
The prevalence of congenital malformations and its correlation with consanguineous marriages.
مقالات الدوريات
19
0
A rare case of familial methemoglobinemia with congenital heart disease.
Nayak, Jhasaketan.
Oman Medical Specialty Board.
2024-05-01
A rare case of familial methemoglobinemia with congenital heart disease.
مقالات الدوريات
0
0
Oculocutaneous albinism associated with Axenfeld's anomaly : three case reports.
Keshav, B. R.
College of Medicine, Sultan Qaboos University.
2010-04
Oculocutaneous albinism associated with Axenfeld's anomaly : three case reports.
مقالات الدوريات
0
0
Nutritional status and cognitive impairment in elderly.
Daradkeh, Ghazi.
Asian Network for Scientific Information.
2014-10
Nutritional status and cognitive impairment in elderly.
مقالات الدوريات
0
0
Profile difference between male and female psychiatric patients seeking certificate of disability.
Balhara, Yatan Pal Singh.
Oman Medical Specialty Board.
2011-11
Profile difference between male and female psychiatric patients seeking certificate of disability.
مقالات الدوريات
0
0
Glucose galactose malabsorption complicated with rickets and nephrogenic diabetes insipidus.
Al-Lawati, Tawfiq
Oman Medical Specialty Board.
2008-07
Glucose galactose malabsorption complicated with rickets and nephrogenic diabetes insipidus.
مقالات الدوريات
0
0
Congenital nasal pyriform aperture Stenosis : first case report in Oman.
Al-Abri, Rashid.
Oman Medical Specialty Board.
2008-07
Congenital nasal pyriform aperture Stenosis : first case report in Oman.
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