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10. A case of HB J-Meerut (or Hb J-Birmingham) [alpha 120(H3)Ala-->Glu]. Yalçin A; Avcu F; Beyan C; Gürgey A; Ural AU Hemoglobin; 1994 Nov; 18(6):433-5. PubMed ID: 7713747 [No Abstract] [Full Text] [Related]
11. Hereditary hemolytic disorders. Jaffé ER Bull N Y Acad Med; 1970 Jun; 46(6):397-410. PubMed ID: 5267233 [No Abstract] [Full Text] [Related]
12. [Genotypic anemia in young infants]. Polonovski C J Sci Med Lille; 1970 Jan; 88(1):1-23. PubMed ID: 5435298 [No Abstract] [Full Text] [Related]
13. [Congenital hemolytic anemia with intra-erythrocytic inclusions and black urine]. MOZZICONACCI P; BESSIS M; MALASSENET R; ATTAL C; PHAM-HUU-TRUNG ; RAPPAPORT R Ann Pediatr (Paris); 1962; 38():349-54. PubMed ID: 14476789 [No Abstract] [Full Text] [Related]
14. First report of successful treatment for hemoglobin Bristol-Alesha by hemopoietic stem cell transplantation. Li S; Chen K; Huang C; Zhang N; Jiang H; Jiang S Ann Hematol; 2022 Mar; 101(3):617-619. PubMed ID: 34851438 [TBL] [Abstract][Full Text] [Related]
15. [The first case of Hb Camden carriage in Russia]. Aseeva EA; Lutsenko IN; Pivnik AV; Spivak VA; Beliaeva LS; Kremenetskaia AM; Saad V Ter Arkh; 1993; 65(7):49-51. PubMed ID: 8211780 [TBL] [Abstract][Full Text] [Related]
16. [Peculiar genetic aspects of hemoglobin H-microcythemia in a familial strain of Sardinian subjects]. Sulis E; Alessio L; Pabis A; Piras GC Boll Soc Ital Biol Sper; 1967 Jul; 43(14):839-42. PubMed ID: 6056686 [No Abstract] [Full Text] [Related]
17. [Dyserythropoietic congenital anemia. Hematological and chromosomal study of a case]. Sansone G Haematologica; 1972; 57(9):587-90. PubMed ID: 4199315 [No Abstract] [Full Text] [Related]
18. [Hereditary blood diseases]. Ikkala E Duodecim; 1968; 84(6):434-48. PubMed ID: 5671647 [No Abstract] [Full Text] [Related]
19. Hereditary hemolytic disorders among the Ashram school children in Mayurbhanj district of Orissa. Balgir RS; Murmu B; Dash BP J Assoc Physicians India; 1999 Oct; 47(10):987-90. PubMed ID: 10778694 [TBL] [Abstract][Full Text] [Related]
20. [Congenital type 2 dyserythropoiesis. 2 familial cases revealed by neonatal hemolytic anemia]. Bachelot C; Rambaud P; Déchelette E; Dieterlen M; Mouriquand C; Beaudoing A Pediatrie; 1973; 28(5):495-503. PubMed ID: 4766778 [No Abstract] [Full Text] [Related] [Next] [New Search]