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عدد العناصر المسترجعة: 8
Oman Medical Specialty Board
Mutation
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مقالات الدوريات
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Dystonia in ataxia telangiectasia : a case report with novel mutations.
Zaki-Dizaji, Majid.
Oman Medical Specialty Board.
2020-01
Dystonia in ataxia telangiectasia : a case report with novel mutations.
مقالات الدوريات
0
0
Phenotype expression variability in children with GABRB3 heterozygous mutations.
Khair, Abdulhafeez M.
Oman Medical Specialty Board.
2021-03
Phenotype expression variability in children with GABRB3 heterozygous mutations.
مقالات الدوريات
0
0
Occurrence of optic neuritis and cervical cord schwannoma with Charcot-Marie-tooth Type 4B1disease.
Scott, Patrick.
Oman Medical Specialty Board.
2016-05
Occurrence of optic neuritis and cervical cord schwannoma with Charcot-Marie-tooth Type 4B1disease.
مقالات الدوريات
0
0
Thyroid hormone resistance due to a Novel De Novo mutation in thyroid hormone receptor alpha : first case report from the Middle East and North Africa.
Al Shidhaniyah, Azza.
Oman Medical Specialty Board.
2021-01
Thyroid hormone resistance due to a Novel De Novo mutation in thyroid hormone receptor alpha : first case report from the Middle East and North Africa.
مقالات الدوريات
0
0
Genetics and pathophysiology of maturity-onset diabetes of the young (MODY) : a review of current trends.
Yahaya, Tajudeen O.
Oman Medical Specialty Board.
2020-05
Genetics and pathophysiology of maturity-onset diabetes of the young (MODY) : a review of current trends.
مقالات الدوريات
0
0
Acrodermatitis enteropathica : a case report.
Al Naamaniyah, Asma.
Oman Medical Specialty Board.
2020-11
Acrodermatitis enteropathica : a case report.
مقالات الدوريات
0
0
Mutation in the PCSK9 gene in Omani Arab subjects with autosomal dominant hypercholesterolemia and its effect on PCSK9 protein structure.
Al-Waili, Khalid.
Oman Medical Specialty Board.
2013-01
Mutation in the PCSK9 gene in Omani Arab subjects with autosomal dominant hypercholesterolemia and its effect on PCSK9 protein structure.
مقالات الدوريات
1
0
A novel cystic fibrosis gene mutation C.4242+1G>C in an Omani patient : a case Report.
Al-Balushi, Said.
Oman Medical Specialty Board.
2021-03
A novel cystic fibrosis gene mutation C.4242+1G>C in an Omani patient : a case Report.
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Oman Medical Specialty Board
Mutation
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Al-Balushi, Said.
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(1)
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