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25. [Hereditary sideroblastic anemia in 3 Canary Island families]. Malcorra JJ; Balda MI; Campo C; Negrín M Sangre (Barc); 1991 Aug; 36(4):332-3. PubMed ID: 1776117 [No Abstract] [Full Text] [Related]
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28. [Pathogenic gene linkage analysis and hemopoietic characteristics in a kindred with sideroblastic anemia]. Zhu P; Wang M; Shi Y; Xue H; Yu J; Ma M; Bu D Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Feb; 16(1):22-5. PubMed ID: 9949236 [TBL] [Abstract][Full Text] [Related]
30. Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages. Notarangelo LD; Parolini O; Albertini A; Duse M; Mazzolari E; Plebani A; Camerino G; Ugazio AG Hum Genet; 1991 Dec; 88(2):130-4. PubMed ID: 1757090 [TBL] [Abstract][Full Text] [Related]
31. Three patients with structurally abnormal X chromosomes, each with Xq13 breakpoints and a history of idiopathic acquired sideroblastic anemia. Dewald GW; Pierre RV; Phyliky RL Blood; 1982 Jan; 59(1):100-5. PubMed ID: 7053756 [TBL] [Abstract][Full Text] [Related]
33. Sideroblastic anaemia. May A; Fitzsimons E Baillieres Clin Haematol; 1994 Dec; 7(4):851-79. PubMed ID: 7881157 [TBL] [Abstract][Full Text] [Related]
34. Genetic localisation of mental retardation with spastic diplegia to the pericentromeric region of the X chromosome: X inactivation in female carriers. Martínez F; Tomás M; Millán JM; Fernández A; Palau F; Prieto F J Med Genet; 1998 Apr; 35(4):284-7. PubMed ID: 9598720 [TBL] [Abstract][Full Text] [Related]
35. Leber hereditary optic neuropathy: estimation of number of embryonic precursor cells and disease threshold in heterozygous affected females at the X-linked locus. Bu X; Rotter JI Clin Genet; 1992 Sep; 42(3):143-8. PubMed ID: 1395084 [TBL] [Abstract][Full Text] [Related]
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