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مقالات الدوريات
0
0
Coexistence of autism spectrum disorders among three children with tuberous sclerosis complex : case reports and review of literature.
Al-Futaisiyah, Amna.
College of Medicine, Sultan Qaboos University.
2016-11
Coexistence of autism spectrum disorders among three children with tuberous sclerosis complex : case reports and review of literature.
مقالات الدوريات
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.
مقالات الدوريات
1
0
Variations in Arabic reading skills between normally achieving and at risk for reading disability students in second and fourth grades.
Emam, Mahmoud.
Canadian Center of Science and Education.
2014-08
Variations in Arabic reading skills between normally achieving and at risk for reading disability students in second and fourth grades.
مقالات الدوريات
1
0
Novel mutation in Wolcott–Rallison syndrome with variable expression in two Omani siblings.
Al-Sinaniyah, Siham.
Oman Medical Specialty Board.
2015-03
Novel mutation in Wolcott–Rallison syndrome with variable expression in two Omani siblings.
مقالات الدوريات
6
0
A SWOT analysis of parent-mediated intervention for children with autism spectrum disorder : Oman as a regional model.
Idris, Ahmed B.
Taylor and Francis Ltd.
2022-01-01
A SWOT analysis of parent-mediated intervention for children with autism spectrum disorder : Oman as a regional model.
مقالات الدوريات
0
0
Consanguinity, endogamy and inborn errors of metabolism in Oman : a cross-sectional study.
Al-Thihli, Khalid.
S. Karger AG.
2014-07
Consanguinity, endogamy and inborn errors of metabolism in Oman : a cross-sectional study.
مقالات الدوريات
0
0
Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family.
Al-Amri, Ahmed.
Wiley.
2016-07
Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family.
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النص الكامل فقط
اللغة
الأنجليزية
(7)
الفئة
مقالات الدوريات
(7)
تاريخ النشر
المجموعة
مقالات الدوريات
(6)
الموضوع
Autism spectrum disorders--Oman--Case reports
(2)
Arabic language--Study and teaching--Oman
(1)
Autism spectrum disorders--Oman
(1)
Chromosome abnormalities--Oman--Case reports
(1)
Consanguinity--Oman
(1)
Diabetes--Oman
(1)
Endogamy and exogamy--Oman
(1)
Head--Abnormalities--Diagnosis--Oman--Case reports
(1)
Intellectual disability--Genetic aspects--Oman
(1)
Medical genetics--Oman--Case reports
(1)
Metabolism, Inborn errors of--Oman
(1)
Osteochondrodysplasia--Oman
(1)
Pancreas--Diseases
(1)
Pancreas--Diseases--Oman
(1)
Reading disability--Oman
(1)
Tuberous sclerosis--Oman--Case reports
(1)
Wolcott–Rallison syndrome--Oman
(1)
المؤلف
Al-Amri, Ahmed.
(1)
Al-Futaisiyah, Amna.
(1)
Al-Sinaniyah, Siham.
(1)
Al-Thihli, Khalid.
(1)
Emam, Mahmoud.
(1)
Idris, Ahmed B.
(1)
Udayakumar, Achandira M.
(1)
الناشر
College of Medicine Sultan Qaboos University
(2)
Canadian Center of Science and Education
(1)
Oman Medical Specialty Board
(1)
S Karger AG
(1)
Taylor and Francis Ltd
(1)
Wiley
(1)
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