Prenatal diagnosis of HbE-Lepore and Hb Lepore-β-thalassemia: the importance of accurate genotyping of the couple at risk
Author:
Affiliation:
1. National Institute of Immunohematology; Mumbai; India
2. Foundation for Research in Genetics and Endocrinology (FRIGE); Institute of Human Genetics; Ahmedabad; India
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference12 articles.
1. Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western India;Madan;Indian J Hum Genet,2010
2. The Molecular Pathology of the Thalassaemias
3. Hb Lepore-Leiden: a new δ/β rearrangement associated with a β-thalassemia minor phenotype;Harteveld;Hemoglobin,2008
4. The first case of Hb E-Saskatoon associated with Hb Lepore-Baltimore found in Spain;Ropero;Hemoglobin,2005
5. Identification of Hb Lepore-Washington-Boston in association with Hb E [β26(B8)Glu----Lys] in a Thai female;Boontrakoonpoontawee;Hemoglobin,1987
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1. Compound Heterozygote Hemoglobin Lepore-Baltimore Haplotype with β-Thalassemia;Indian Journal of Pediatrics;2021-03-10
2. The phenotypic and molecular diversity of hemoglobinopathies in India: A review of 15 years at a referral center;International Journal of Laboratory Hematology;2018-11-29
3. Prenatal Diagnosis of HbE-β-Thalassemia: Experience of a Center in Western India;Indian Journal of Hematology and Blood Transfusion;2017-09-04
4. beta-Thalassemia Intermedia Caused by Compound Heterozygosity for Hb Lepore-Hollandia and beta-Thalassemia is Rare in the Indian Population;HEMOGLOBIN;2015
5. Hemoglobin variants and high-performance liquid chromatography;International Journal of Laboratory Hematology;2013-01-11
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