FANCG 637-643 deletion mutation: frequency in black patients with acute myeloid leukaemia or aplastic anaemia and the clinical phenotype of homozygotes

FANCG 637-643 deletion mutation: frequency in black patients with acute myeloid leukaemia or aplastic anaemia and the clinical phenotype of homozygotes

Student Number : 9807768F - MSc (Med) research report - Faculty of Health Sciences === Fanconi anaemia (FA) is an autosomal recessive disorder characterised by aplastic anaemia (AA) and a high risk of developing acute myeloid leukaemia (AML). It is unknown whether heterozygote carriers are also...

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Bibliographic Details
Main Author: Haw, Tabitha
Format: Others
Language:en
Published: 2006
Subjects:
Fanconi anaemia
FA
autosomal recessive disorder
aplastic anaemia
acute myeloid leukaemia
AML
black South African population
FANCG 637-643
congenital abnormalities
Online Access:http://hdl.handle.net/10539/1881

Internet

http://hdl.handle.net/10539/1881

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