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Dergiler / Turkish Journal of Hematology / 2009 / Cilt: 26 - Sayı: 1

Familial thrombocytopenia associated with ovarian agenesis, umbilical hernia, bicuspid aortic valve, patent ductus arteriosus and epilepsia

Ayşe Nur TORUN
Alptekin GÜRSOY
Neslihan Başçıl TÜTÜNCÜ
Nilgün Güvener DEMİRAĞ
Sayfa
42–43
DOI
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TORUN, A. N., GÜRSOY, A., TÜTÜNCÜ, N. B., DEMİRAĞ, N. G. (2009). Familial thrombocytopenia associated with ovarian agenesis, umbilical hernia, bicuspid aortic valve, patent ductus arteriosus and epilepsia. Turkish Journal of Hematology, Cilt: 26 - Sayı: 1, 42–43. https://ajindex.com/articles/413364

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Kaynakça (5)

  1. Balduini CL, Iolascon A, Savoia A. Inherited thrombocytopenias: from genes to therapy. Haematologica 2002;87:860-80
  2. Geddis AE, Kaushansky K. Inherited thrombocytopenias: toward a molecular understanding of disorders of platelet production. Curr Opin Pediatr 2004;16:15-22
  3. Shprintzen RJ, Goldberg RB, Young D, Wolford L. The velo-cardio-facial syndrome: a clinical and genetic analysis. Pediatrics 1981;67:167-72
  4. Obregon MG, Mingarelli R, Digilio MC, Zelante L, Giannotti A, Sabatino G, Dallapiccola B. Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patients. Ann Genet 1992;35:208-12
  5. Lalwani AK, Goldstein JA, Kelley MJ, Luxford W, Castelein CM, Mhatre AN. Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9. Am J Hum Genet 2000;67:1121-8.