These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
220 related items for PubMed ID: 7803273
1. Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil. Saad ST, Costa FF, Vicentim DL, Salles TS, Pranke PH. Br J Haematol; 1994 Oct; 88(2):295-9. PubMed ID: 7803273 [Abstract] [Full Text] [Related]
5. Combined ankyrin and spectrin deficiency in hereditary spherocytosis. Pekrun A, Eber SW, Kuhlmey A, Schröter W. Ann Hematol; 1993 Aug; 67(2):89-93. PubMed ID: 8347735 [Abstract] [Full Text] [Related]
6. Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases. Iolascon A, Miraglia del Giudice E, Camaschella C, Pinto L, Nobili B, Perrotta S, Cutillo S. Br J Haematol; 1991 Aug; 78(4):551-4. PubMed ID: 1832935 [Abstract] [Full Text] [Related]