Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal A TIndian(AATAAA>AATA– –) Mutation in Four Indian Families

Heterogeneity of Hemoglobin H Disease in Childhood

(2011) Ashutosh Lal et al.   NEW ENGLAND JOURNAL OF MEDICINE

Molecular Diversity of Hemoglobin H Disease in India: Table 1

(2010) Anita H. Nadkarni et al.   AMERICAN JOURNAL OF CLINICAL PATHOLOGY

Hb H Disease Due to Homozygosity for a Rare α2-Globin Variant, Hb Sallanches

(2010) Prashant Warang et al.   HEMOGLOBIN

α-thalassaemia

(2010) Cornelis L Harteveld et al.   Orphanet Journal of Rare Diseases

Hemoglobin H-constant spring in North America: An alpha thalassemia with frequent complications

(2009) Sylvia Titi Singer et al.   AMERICAN JOURNAL OF HEMATOLOGY

Clinical features and molecular analysis in Thai patients with HbH disease

(2009) Vichai Laosombat et al.   ANNALS OF HEMATOLOGY

The Alpha Thalassaemias

(2008) D. R. Higgs et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Polymerase Chain Reaction-Based Search for Two α-Globin Gene Mutations in India

(2008) Gargi Bhattacharya et al.   HEMOGLOBIN

Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia

(2008) Henri Wajcman et al.   HEMOGLOBIN