Rapid diagnosis of β thalassemia mutations in mediterraneans by PCR and restriction analysis of natural or created sites-Reference-Cited by-同舟云学术

Rapid diagnosis of β thalassemia mutations in mediterraneans by PCR and restriction analysis of natural or created sites

Published:1997-07 Issue:5 Volume:30 Page:433-437
ISSN:0009-9120
Container-title:Clinical Biochemistry
language:en
Short-container-title:Clinical Biochemistry

Author:

Denmat Corinne Le,Duchassaing Danielle

Publisher

Elsevier BV

Subject

Clinical Biochemistry,General Medicine

Reference14 articles.

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3. Prenatal diagnosis of β thalassemia based on restriction analysis of amplified fetal DNA;Pirastu;J Med Genet,1989

4. Analysis of enzymatically amplified β-globin and HLA DQa DNA with allele specific oligonucleotide probes;Saiki;Nature,1986

5. Rapid and direct detection of the most frequent Mediterranean R thalassemic mutations by multiplex allele specific enzymatic amplification;Bienvenu;Hum Biol,1992

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1. Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC);Journal of Clinical Laboratory Analysis;2016-04-18

2. ?-globin gene cluster haplotypes associated with ?-thalassemia on Corsica island;American Journal of Hematology;2004

3. Detection of β-thalassemia by a DNA piezoelectric biosensor coupled with polymerase chain reaction;Analytica Chimica Acta;2003-03

4. Rapid detection of the major Mediterranean β-thalassaemia mutations by real-time polymerase chain reaction using fluorophore-labelled hybridization probes;British Journal of Haematology;2002-10-30

5. β-Thalassemia Mutations in Corsica;Hemoglobin;2000-01