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Results 1 - 10 of 51 for Thrombocytopenia 10
  1. X-linked thrombocytopenia 
    ... of thrombocytopenia. The estimated incidence of X-linked thrombocytopenia is between 1 and 10 per million males worldwide; this condition is rarer ... families with Wiskott-Aldrich syndrome and X-linked thrombocytopenia. Pathology. ... 10.1080/00313020410001692521. Citation on PubMed Imai K, Morio ...
    https://medlineplus.gov/genetics/condition/x-linked-thrombocytopenia - Genetics
  2. Immune thrombocytopenia 
    ... D, Newland AC. Current Management of Primary Immune Thrombocytopenia. Adv Ther. 2015 Oct;32(10):875-87. doi: 10.1007/s12325-015-0251- ... on the investigation and management of primary immune thrombocytopenia. Blood. 2010 Jan 14;115(2):168-86. doi: 10.1182/blood-2009-06-225565. Epub 2009 Oct ...
    https://medlineplus.gov/genetics/condition/immune-thrombocytopenia - Genetics
  3. Thrombocytopenia-absent radius syndrome 
    ... No abstract available. Citation on PubMed Toriello HV. Thrombocytopenia-absent radius syndrome. Semin Thromb Hemost. 2011 Sep;37(6):707-12. doi: 10.1055/s-0031-1291381. Epub 2011 Nov 18. ...
    https://medlineplus.gov/.../thrombocytopenia-absent-radius-syndrome - Genetics
  4. GNE gene 
    ... Mutation in GNE is associated with severe congenital thrombocytopenia. Blood. 2018 Oct 25;132(17):1855-1858. doi: 10.1182/blood-2018-04-847798. Epub 2018 Jun ...
    https://medlineplus.gov/genetics/gene/gne - Genetics
  5. Dyserythropoietic anemia and thrombocytopenia 
    ... PD, Balamohan SM, Raskind WH, Kacena MA. Inherited thrombocytopenia due to GATA-1 mutations. Semin Thromb Hemost. 2011 Sep;37(6):682-9. doi: 10.1055/s-0031-1291378. Epub 2011 Nov 18. ...
    https://medlineplus.gov/...rythropoietic-anemia-and-thrombocytopenia - Genetics
  6. NBEAL2 gene 
    ... phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and alpha-granule deficiency. Haematologica. 2013 Jun;98(6):868-74. doi: 10.3324/haematol.2012.075861. Epub 2012 Oct 25. ...
    https://medlineplus.gov/genetics/gene/nbeal2 - Genetics
  7. Gray platelet syndrome 
    ... phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and alpha-granule deficiency. Haematologica. 2013 Jun;98(6):868-74. doi: 10.3324/haematol.2012.075861. Epub 2012 Oct 25. ...
    https://medlineplus.gov/genetics/condition/gray-platelet-syndrome - Genetics
  8. ITGB3 gene 
    ... L718P mutation in a pedigree with autosomal dominant thrombocytopenia with anisocytosis. Br J Haematol. 2013 Feb;160(4):521-9. doi: 10.1111/bjh.12160. Epub 2012 Dec 17. Citation ...
    https://medlineplus.gov/genetics/gene/itgb3 - Genetics
  9. Chromosome 1 
    ... resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome. Am J Hum Genet. 2007 Feb;80(2):232-40. doi: 10.1086/510919. Epub 2006 Dec 21. Citation on ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
  10. X chromosome 
    ... idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, and thrombocytopenia segregating as an X linked recessive disorder. J Med Genet. 1997 Aug;34(8):666-9. doi: 10.1136/jmg.34.8.666. Citation on PubMed ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics
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