Benign familial macrocytosis

Clinical and Laboratory Haematology

Volumn 18, Issue 1, 1996, Pages 41-43

  Sechi, L A ^a   De Carli, S ^a   Catena, C ^a   Zingaro, L ^a   Bartoli, E ^a  

^a UNIVERSITY OF UDINE   (Italy)

Author keywords

folic acid; macrocytosis; vitamin B12

Indexed keywords

CYANOCOBALAMIN; FOLIC ACID; HEMOGLOBIN;

ADULT; ARTICLE; BONE MARROW CELL; CASE REPORT; FEMALE; HUMAN; HUMAN CELL; MEGALOCYTOSIS; PRIORITY JOURNAL;

EID: 0030003696     PISSN: 01419854     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-2257.1996.tb00736.x     Document Type: Article

References (9)

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3. Fox R.M., Wood M.H., Royse-Smith D. & O'Sullivan W.J. (1973) Heredity orotic aciduria: types I and II. American Journal of Medicine 55, 791-798.
4. Hakami N., Nelman P.E., Canellos G.P. & Lazerson J. (1971). Neonatal megaloblastic anemia due to inherited transcobalamin II deficiency in two siblings. New England Journal of Medicine 285, 1163-1170.
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6. McPhedran P., Barnes M.G., Weinstein J.S. & Robertson J.S. (1973) Interpretation of electronically determined macrocytosis. Annals of Internal Medicine 78, 677-683.
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9. Walters T.R. (1967) Congenital megaloblastic anemia responsive to N-formyl-tetrahydrofolic acid administration. Journal of Pediatrics 70, 686-689.