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Journal articles
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Fatal cardiac arrhythmia and long-qt syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (cgl4) due to ptrf-cavin mutations.
Rajab, Anna.
Elsevier B. V.
2010-03
Fatal cardiac arrhythmia and long-qt syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (cgl4) due to ptrf-cavin mutations.
Journal articles
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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.
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antifouling
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Bioactive Compounds
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biofilms
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Birth head circumference
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chemical defence
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Fishes--Arabian Gulf
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FTO protein, Human
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Genetic polymorphism
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Health-related quality of life
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Hemoglobin
(1)
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Long QT syndrome--Oman
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Magnetic Resonance Imaging
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Melanocortin-4 receptor
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Red Sea
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Author
Safaie, Mohsen.
(2)
Akasha, Bilal.
(1)
Al-Saleh, Mohsen Mohammed Taqi Mohsen
(1)
Ardakani, Mostafa K.
(1)
Dehghani, Mohsen.
(1)
Forghani, Foroogh.
(1)
Gadhi, Alaa Aref Abdullah.
(1)
Ghayoumi, Razieh.
(1)
Hennies, Hans Christian.
(1)
Iraji, Fariba.
(1)
Kaki, Abdullah.
(1)
Mahmoud, Touka M. A.
(1)
Mirzaei, Mojtaba.
(1)
Mohseni, Raheleh.
(1)
Mozafarizadeh, Mina.
(1)
Rajab, Anna.
(1)
Rostamzadeh, Ayoob.
(1)
Samimi, Mansooreh.
(1)
Taghizadeh, Mohsen.
(1)
Yousefkhani, Seyyed Saeed Hosseinian.
(1)
Zamharir, Maryam Ghayeb.
(1)
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Oman Medical Specialty Board
(7)
BioMed Central
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American Society of Human Genetics
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Cambridge University Press
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College of Medicine Sultan Qaboos University
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Elsevier
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Elsevier B V
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Elsevier Ltd
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Institute of Electrical and Electronics Engineers…
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IWA Publishing
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Oman Medical Speciality Board
(1)
Pensoft Publishers
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Sultan Qaboos University
(1)
جامعة السلطان قابوس كلية العلوم الزراعية والبحرية
(1)
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