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2023 | 1 |
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Identification of Extremely Rare Pathogenic CNVs by Array CGH in Saudi Children with Developmental Delay, Congenital Malformations, and Intellectual Disability.
Children (Basel). 2023 Mar 31;10(4):662. doi: 10.3390/children10040662.
Children (Basel). 2023.
PMID: 37189911
Free PMC article.
An SP1-binding site polymorphism in the COLIAI gene and osteoporosis in Egyptian patients with thalassemia major.
Hamed HM, Galal A, Ghamrawy ME, Abd El Azeem K, Hussein IR, Abd-Elgawad MF.
Hamed HM, et al. Among authors: hussein ir.
Blood Coagul Fibrinolysis. 2011 Mar;22(2):81-5. doi: 10.1097/MBC.0b013e32834248fb.
Blood Coagul Fibrinolysis. 2011.
PMID: 21178584
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