A second type of hereditary persistence of foetal haemoglobin in India

Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia.

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Clinical, hematological, and molecular features in Sicilians with Hb S-beta-thalassemia.

American journal of hematology·1992

Molecular characterization of beta-thalassemia in Azerbaijan.

Human genetics·1992

Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin.

American journal of hematology·1992

Heterogeneity of the hemoglobin of the Ohrid trout (Salmo L. typicus).

Biochemical genetics·1992

Haplotypes in SS patients from Nigeria; characterization of one atypical beta S haplotype no. 19 (Benin) associated with elevated HB F and high G gamma levels.

Annals of hematology·1992

Hyperdiploid multiple myeloma: A heterogeneous entity requiring refined risk stratification-Insights from chromosome count and cytogenetic abnormalities.

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Pancreatic iron overload as a marker of endocrine complications in transfusion-dependent thalassaemia: A multicentre study.

British journal of haematology·2026

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Sickle cell anaemia with and without crises: An observational study of pregnancy outcomes.

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Kerion, an often missed scalp lesion: A case report.

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Prognostic significance of monotypic plasma cell infiltration of the bone marrow in patients with Waldenström macroglobulinemia.

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A second type of hereditary persistence of foetal haemoglobin in India

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Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia.

Clinical, hematological, and molecular features in Sicilians with Hb S-beta-thalassemia.

Molecular characterization of beta-thalassemia in Azerbaijan.

Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin.

Heterogeneity of the hemoglobin of the Ohrid trout (Salmo L. typicus).

Haplotypes in SS patients from Nigeria; characterization of one atypical beta S haplotype no. 19 (Benin) associated with elevated HB F and high G gamma levels.

Hyperdiploid multiple myeloma: A heterogeneous entity requiring refined risk stratification-Insights from chromosome count and cytogenetic abnormalities.

A phase IIa study of the anti-PD-L1 antibody avelumab in relapsed/refractory PTCL: The AVAIL-T trial.

Interplay between fibroblast growth factor 9 (FGF9) and CD44 underlies 46,XY disorders of sex development in Kruppel-like factor 1 (KLF-1)-E325K-associated congenital dyserythropoietic anaemia (CDA-IV).

Pancreatic iron overload as a marker of endocrine complications in transfusion-dependent thalassaemia: A multicentre study.

Reduced-dose versus standard-dose total body irradiation before allogeneic haematopoietic stem cell transplantation in adults with acute lymphoblastic leukaemia.

Sickle cell anaemia with and without crises: An observational study of pregnancy outcomes.

Fournier's Gangrene and Extensive Abdominal Necrotizing Fasciitis Secondary to Perforated Appendicitis Within an Inguinoscrotal Hernia: A Rare Case Report.

Kerion, an often missed scalp lesion: A case report.

Prognostic significance of monotypic plasma cell infiltration of the bone marrow in patients with Waldenström macroglobulinemia.

Staphylococcus pettenkoferi: an underrecognized species with clinically relevant antimicrobial resistance. A comprehensive genomic European study.

Isolated Tuberculous Testicular Abscess Without Systemic Involvement: A Rare Cause of Scrotal Swelling.

Retraction: MicroRNAs, long non-coding RNAs, and circular RNAs and gynecological cancers: focus on metastasis.

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A second type of hereditary persistence of foetal haemoglobin in India

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