Hemoglobin H disease: not necessarily a benign disorder
- 1 February 2003
- journal article
- review article
- Published by American Society of Hematology in Blood
- Vol. 101 (3) , 791-800
- https://doi.org/10.1182/blood-2002-07-1975
Abstract
Doi:10.1182/blood-2002-07-1975 Hemoglobin H disease: not necessarily a benign disorder Updated information and services can be found atKeywords
This publication has 130 references indexed in Scilit:
- Phenotypic and molecular diversity of haemoglobin H disease: a Greek experienceBritish Journal of Haematology, 2000
- Genetic and Clinical Features of Hemoglobin H Disease in Chinese PatientsNew England Journal of Medicine, 2000
- Risk of neural tube defects in the offspring of thalassaemia carriers in Hong Kong ChinesePrenatal Diagnosis, 1999
- Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domainNature Genetics, 1997
- Atypical HbH disease in a Surinamese patient resulting from a combination of the −SEA and −α3.7 deletions with HbC heterozygosityBritish Journal of Haematology, 1997
- The α-Thalassemia/Mental Retardation SyndromesMedicine, 1996
- The interaction of α° thalassaemia with Hb Icaria: three unusual cases of haemoglobinopathy HBritish Journal of Haematology, 1996
- A new deletional α-thalassemia detected in yemenites with hemoglobin H diseaseAmerican Journal of Hematology, 1994
- Identification of an extensive ζ‐α globin gene deletion in a Chinese individualBritish Journal of Haematology, 1992
- Hb H Disease Caused by a Homozygosity for the AATAAA→ AATAAG Mutation in the Polyadenylation Site of the α2-Globin Gene: Hematological ObservationsActa Haematologica, 1992