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Manal Wilson
Manal Wilson
Cairo University
Medicine
Internal medicine
Polymorphism (computer science)
Genotype
Endocrinology
7
Papers
35
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Alpha-Smooth Muscle Actin (a-SMA) Gene, a Possible Derive of Myofibroblasts in Bone Marrow Fibrosis
2020
Amira Osama Abd El-Ghafar
Amal El-Mahdy
Samea Rizk
Howayda Mohamed
Hanan El-Hosseiny
Manal Wilson
Amira Noureldin
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Novel marker for the detection of sickle cell nephropathy: soluble FMS-like tyrosine kinase-1 (sFLT-1)
2015
Pediatric Nephrology
Ilham Youssry
Samuel H Makar
Rania Fawzy
Manal Wilson
Ghada AbdAllah
Eman Fathy
Happy Sawires
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Citations (10)
Study of the effect of HFE gene mutations on iron overload in Egyptian thalassemia patients
2015
the egyptian journal of medical human genetics
Manal Wilson
Hanan Al-Wakeel
Fadwa Said
Mona El-Ghamrawy
Mary Assaad
Amal El Beshlawy
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Citations (4)
Glutathione S transferase theta1 and mu1 gene polymorphisms and phenotypic expression of asthma in Egyptian children: a case–control study
2014
Italian Journal of Pediatrics
Nihal Mohamed Mohamed El Rifai
Nadia Moustafa
Nelly Degheidy
Manal Wilson
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Citations (8)
Study of the Effect of HFE Gene Mutations on Iron Overload in Egyptian Thalassemia Patients
2014
Blood
Amal El Beshlawy
Manal Wilson
Elwakeel Hanan
Mona Elghmarwy
Fadwa Said
Mary Assaad
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