PMID: 6111635Mar 7, 1981Paper
Molecular basis for mild forms of homozygous beta-thalassaemia
Lancet
D J WeatherallJ B Clegg
Abstract
Five Cypriots homozygous for beta +-thalassaemia have inherited deletion or non-deletion forms of alpha-thalassaemia that seem to have modified the usually severe clinical picture to that of mild thalassaemia intermedia. These observations have important implications for the antenatal diagnosis of beta-thalassaemia.
Citations
Apr 1, 1991·Annals of Hematology·D Loukopoulos
May 1, 1991·Annals of Hematology·D Loukopoulos
Jan 1, 1989·Neurosurgical Review·J Reif, N Graf
Sep 1, 1984·Indian Journal of Pediatrics·D K ShomeD Mohanty
Oct 26, 2012·Analytical and Bioanalytical Chemistry·Guido CrisponiAndrea Tapparo
Jun 4, 1983·Lancet·J S WainscoatS H Orkin
Mar 1, 1983·British Journal of Haematology·J S WainscoatD J Weatherall
Apr 1, 1993·British Journal of Haematology·P WinichagoonP Wasi
Jan 1, 1990·Annals of the New York Academy of Sciences·A CaoR Galanello
May 1, 1995·Archives of Disease in Childhood·S RatipB Modell
Dec 1, 1982·Journal of Medical Genetics·M A ZagoC Bottura
Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study.
Apr 1, 2010·BMC Medical Genetics·Richard ShervaLindsay A Farrer
Jun 11, 2005·European Journal of Haematology·Sanmay BandyopadhyayUma B Dasgupta
Aug 31, 2006·British Journal of Haematology·Orly Weizer-SternGideon Rechavi
May 1, 1987·British Journal of Haematology·C CamaschellaU Mazza
Oct 22, 2009·Hematology·Vineeta SharmaRenu Saxena
Mar 1, 1988·British Journal of Haematology·D G EfremovT H Huisman
Sep 1, 1986·British Journal of Haematology·V ChanD Todd
Jan 1, 1985·Annals of the New York Academy of Sciences·R A PoppS E Lewis
Jan 1, 1985·Annals of the New York Academy of Sciences·P WasiA Promboon
Jan 1, 1985·Annals of the New York Academy of Sciences·D J WeatherallJ B Clegg
Jun 7, 2006·American Journal of Hematology·Orly Weizer-SternGideon Rechavi
Oct 1, 1994·Prenatal Diagnosis·J S WayeD H Chui
Apr 1, 1982·Prenatal Diagnosis·M FerrariB Brambati
Apr 1, 1983·British Journal of Haematology·M A MelisA Cao
Nov 1, 1982·British Journal of Haematology·E KanavakisT Sophocleous
Nov 1, 1982·British Journal of Haematology·R J TrentD J Weatherall
Mar 13, 2009·Annals of Hematology·Vineeta Sharma, Renu Saxena
Sep 1, 1984·American Journal of Medical Genetics·S FucharoenP Wasi
Apr 3, 2001·Nature Reviews. Genetics·D J Weatherall
Dec 13, 2005·Annals of the New York Academy of Sciences·Eliezer A RachmilewitzZ Ioav Cabantchik
Jan 1, 1983·Human Genetics·P TriadouD Labie
May 24, 2019·ELife·Carinna HockhamFrédéric B Piel
Nov 1, 1985·American Journal of Hematology·P WinichagoonP Wasi
Sep 1, 1999·American Journal of Hematology·I SetianingsihS Forrest
Jan 1, 1982·Hemoglobin·L E Lie-InjoS Vasudevan
Mar 1, 2008·Personalized Medicine·Marina Kleanthous, Marios Phylactides
Jun 18, 1998·Hemoglobin·S F FonsecaF F Costa
Dec 19, 2014·British Journal of Haematology·Bridget S PenmanDavid J Weatherall
Sep 1, 1995·American Journal of Hematology·J S WayeN F Olivieri
Feb 12, 1982·Journal of Chromatography·P BassetJ Rosa
Dec 1, 1987·Blood Reviews·J S WainscoatD J Weatherall
Apr 1, 2008·Archives of Medical Research·Mehryar Habibi RoudkenarMohammad Ali Shokrgozar
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