4.2 Article

Distribution characteristics and clinical phenotype analyses of hemoglobin variants in the Z region of Central Guangxi, Southern China

Related references

Note: Only part of the references are listed.
Article Biochemistry & Molecular Biology

Hb New York, preliminary results concerning the hematologic characteristics and the effects on thalassemia

Zhuru Cheng et al.

Summary: This study found that the hematological characteristics of Hb New York combined with thalassemia are similar to the corresponding thalassemia, and Hb New York does not aggravate the clinical manifestations of thalassemia.

MOLECULAR BIOLOGY REPORTS (2022)

Article Hematology

Molecular epidemiological investigation of abnormal hemoglobin in Shaokwan region, southern China

Hui Yang et al.

Summary: This study investigated the molecular characteristics of abnormal hemoglobin in Shaokwan, Guangdong province. The incidence of hemoglobin variants in this region was found to be 0.46%, with Hb Q-Thailand being the most common variant followed by HbE, Hb NewYork, and Hb G-Chinese.

HEMATOLOGY (2022)

Article Pathology

Why is the novel Hb Miguel Servet visualised by CE-HPLC newborn and not by the CE-HPLC β-thalassaemia programme?

Valle Recasens et al.

Summary: Screening for haemoglobinopathies in newborns can detect new haemoglobin variants, such as Hb Miguel Servet, which can have unexpected findings and require additional testing for accurate identification.

JOURNAL OF CLINICAL PATHOLOGY (2021)

Article Multidisciplinary Sciences

Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China

Hailong Huang et al.

SCIENTIFIC REPORTS (2019)

Review Medicine, General & Internal

Thalassaemia

Ali T. Taher et al.

LANCET (2018)

Article Hematology

Hb Cibeles [α2 CD25(B6) (Gly → Asp)]: a novel alpha chain variant causing alpha-thalassemia

Felix de la Fuente-Gonzalo et al.

INTERNATIONAL JOURNAL OF HEMATOLOGY (2014)