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Platelets Volume 18, 2007 - Issue 4
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Original

Platelet pathology in sex-linked GATA-1 dyserythropoietic macrothrombocytopenia I ultrastructure

James G. White Department of Laboratory Medicine, Pathology and Pediatrics, University of Minnesota School of Medicine, Minneapolis, MN, USACorrespondence[email protected]
, MD,
William L. Nichols Division of Hematology and Internal Medicine, Mayo Clinic, Rochester, MN, USA
&
David P. Steensma Division of Hematology and Internal Medicine, Mayo Clinic, Rochester, MN, USA
Pages 273-283 | Received 31 Aug 2006, Accepted 10 Oct 2006, Published online: 07 Jul 2009

Citations (13)

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Read on this site (5)

James G. White, Kourosh Pakzad & Lynn Meister. (2013) The York platelet syndrome: A fourth case with unusual pathologic features. Platelets 24:1, pages 44-50.
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James G. White, Steven M. Burris & Brian R. Crowe. (2009) GATA-1, G208S macrothrombocytes are deficient in talin: Immunofluorescence studies. Platelets 20:3, pages 216-224.
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J. G. White & A. Thomas. (2009) Platelet structural pathology in a patient with the X-linked GATA-1, R216Q mutation. Platelets 20:1, pages 41-49.
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James G. White. (2007) Platelet pathology in carriers of the X-linked GATA-1 macrothrombocytopenia. Platelets 18:8, pages 620-627.
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James G. White, William L. Nichols & David P. Steensma. (2007) Platelet pathology in sex-linked GATA-1 dyserythropoietic macrothrombocytopenia II. Cytochemistry. Platelets 18:6, pages 436-450.
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Articles from other publishers (8)

Maryam Khan, Raheel Iftikhar, Tariq Ghafoor, Fayyaz Hussain, Qamar un Nisa Chaudhry, Syed Kamran Mahmood, Nighat Shahbaz, Mehreen Ali Khan, Tariq Azam Khattak, Ghassan Umair Shamshad, Jahanzeb Rehman, Sundas Ali, Zunaira Shah, Abdul Rafae, Muhammad Farhan, Faiz Anwer & Parvez Ahmed. (2020) Allogeneic hematopoietic stem cell transplant in rare hematologic disorders: a single center experience from Pakistan. Bone Marrow Transplantation 56:4, pages 863-872.
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Ali Amin Asnafi, Mohammad bagher Mohammadi, Hadi Rezaeeyan, Nader Davari & Najmaldin Saki. (2019) Prognostic significance of mutated genes in megakaryocytic disorders. Oncology Reviews 13:2.
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Tadbir K. Bariana, Willem H. Ouwehand, Jose A. Guerrero & Keith Gomez. (2017) Dawning of the age of genomics for platelet granule disorders: improving insight, diagnosis and management. British Journal of Haematology 176:5, pages 705-720.
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Carlos R. Ferreira, Dong Chen, Shirley M. Abraham, David R. Adams, Karen L. Simon, May C. Malicdan, Thomas C. Markello, Meral Gunay-Aygun & William A. Gahl. (2017) Combined alpha-delta platelet storage pool deficiency is associated with mutations in GFI1B. Molecular Genetics and Metabolism 120:3, pages 288-294.
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Yang Zhou, Qing-Song Dai, Shi-Chang Zhu, Yue-Hua Han, Hai-Long Han, Bo Zhao, Rong-Rong Gao, Jun Zhang & Jing Zhang. (2016) AK048794 maintains the mouse embryonic stem cell pluripotency by functioning as an miRNA sponge for miR-592. Biochemical Journal 473:20, pages 3639-3654.
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Alan B. Cantor. 2016. Molecular and Cellular Biology of Platelet Formation. Molecular and Cellular Biology of Platelet Formation 61 91 .
Belinda K. Singleton, David J. Roxby, John W. Stirling, Frances A. Spring, Carolyn Wilson, Joyce Poole & David J. Anstee. (2012) A novel GATA 1 mutation ( S top414 A rg) in a family with the rare X ‐linked blood group L u(a‐b‐) phenotype and mild macrothrombocytic thrombocytopenia . British Journal of Haematology 161:1, pages 139-142.
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Yuhuan WangRonghua Meng, Vincent HayesRudy FuentesXiang YuCharles S. AbramsHarry F. G. Heijnen, Gerd A. Blobel, Michael S. Marks & Mortimer Poncz. (2011) Pleiotropic platelet defects in mice with disrupted FOG1-NuRD interaction. Blood 118:23, pages 6183-6191.
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