A simple electrophoretic procedure for fetal diagnosis of β-thalassaemia due to short deletions-Reference-Cited by-同舟云学术

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A simple electrophoretic procedure for fetal diagnosis of β-thalassaemia due to short deletions

Published:1992-11 Issue:11 Volume:12 Page:903-907
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Faà V.,Rosatelli M. C.,Sardu R.,Meloni A.,Toffoli C.,Cao A.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference10 articles.

1. Characterization of Three Types of β0-Thaussemia Resulting from a Partial Deletion of the β-Globin Gene

2. [49] DNA analysis in the diagnosis of hemoglobin disorders

3. Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus.

4. Inactivation of an acceptor RNA splice site by a short deletion in beta-thalassemia.

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1. An Early Diagnosis of Thalassemia: A Boon to a Healthy Society;Hemodynamics [Working Title];2021-10-18

2. Revisiting a Complex Rearrangement Involving a 619 Base Pairs Deletion, 6 Nucleotide Insertion Followed by a A > G Substitution Causing β°-Thalassemia;Indian Journal of Hematology and Blood Transfusion;2016-05-26

3. Prenatal Diagnosis of the Hemoglobinopathies;Genetic Disorders and the Fetus;2015-11-23

4. Prenatal Diagnosis of the Hemoglobinopathies;Genetic Disorders and the Fetus;2010-09-24

5. Microsatellite Markers within —SEA Breakpoints for Prenatal Diagnosis of HbBarts Hydrops Fetalis;Clinical Chemistry;2007-02-01

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