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10. [The May-Hegglin anomaly in a family]. Javier G; Millá F; Prats Viñas J; Feliu E Sangre (Barc); 1989 Feb; 34(1):71-3. PubMed ID: 2540536 [No Abstract] [Full Text] [Related]
11. [Intramedullary destruction of blood platelets in a case of familial thrombocytopenia]. Jeanneau C; Tichet M; Boiron M; Caen J Nouv Rev Fr Hematol; 1973; 13(4):515-22. PubMed ID: 4271099 [No Abstract] [Full Text] [Related]
12. [Studies on the platelet volume in children with thrombocytopenia]. Shirahata A; Nakamura T; Asakura A; Tanaka M; Shiiki M Rinsho Ketsueki; 1984 Mar; 25(3):313-21. PubMed ID: 6540823 [No Abstract] [Full Text] [Related]
13. [Hereditary macrothrombocytic thrombocytopenia. Description of a family carrying this anomaly]. Patrone F; Armani U; Boy E; Boccaccio P Haematologica; 1972; 58(9):623-50. PubMed ID: 4206238 [No Abstract] [Full Text] [Related]
14. A pedigree with autosomal dominant thrombocytopenia, red cell macrocytosis, and an occurrence of t(12:21) positive pre-B acute lymphoblastic leukemia. Escher R; Wilson P; Carmichael C; Suppiah R; Liu M; Kavallaris M; Cannon P; Michaud J; Scott HS Blood Cells Mol Dis; 2007; 39(1):107-14. PubMed ID: 17434765 [TBL] [Abstract][Full Text] [Related]
15. [Hematological and genetic investigations of a family affected with May-Hegglin anomaly]. Boreux G; Rudolf H; Miescher PA; Klein D Arch Genet (Zur); 1975; 48(1):47-9. PubMed ID: 1221968 [No Abstract] [Full Text] [Related]
16. A familial platelet disease--hereditary thrombasthenic-thrombopathic thrombocytopenia. Seip M; Kjaerheim A Scand J Clin Lab Invest; 1965; 17():Suppl 84:159+. PubMed ID: 5893276 [No Abstract] [Full Text] [Related]
18. [The thrombocyte counts in healthy premature babies (author's transl)]. Schulz P; Alberts C; Künzer W Klin Padiatr; 1974 Jul; 186(4):280-6. PubMed ID: 4472481 [No Abstract] [Full Text] [Related]
19. [Platelets in biology and pathology during foetal and neonatal period (author's transl)]. Shirahata A; Nojiri K Rinsho Ketsueki; 1982 Jan; 23(1):1-12. PubMed ID: 7047798 [No Abstract] [Full Text] [Related]
20. A patient with pituitary growth hormone deficiency and May-Hegglin anomaly: a distinct entity? Gerver WJ; Neucker AV; Schrander-Stumpel CT Genet Couns; 1994; 5(3):307-10. PubMed ID: 7811433 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]