Unexplained recurrent venous thrombosis in a patient with MYH 9-related disease

By Heller Paula G.   Pecci Alessandro   Glembotsky Ana C.   Savoia Anna   Negro Fernando D.   Balduini Carlo L.   Molinas Felisa C.  

Platelets, Vol. 17, Iss. 4, 2006-06 ,pp. : 274-275

Informa Healthcare

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Association of MYH9/APOL1 with chronic kidney disease in a UK population

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Oxford University Press

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Polymorphisms in the Interleukin-6 Receptor Gene (Asp358Ala) and Body Mass Index in Chilean Women with Type 1 Diabetes

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A family with bolzano-type Bernard–Soulier syndrome carries a benign A1939T MYH9 mutation

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Identification and Molecular Characterization of a Novel Splice-Site Mutation ( G1205C ) in the SQSTM1 Gene Causing Paget’s Disease of Bone in an Extended American Family

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Calcified Tissue International, Vol. 79, Iss. 5, 2006-11 ,pp. : 281-288

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