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A successful strategy for preimplantation genetic diagnosis of myotonic dystrophy using multiplex fluorescent PCR

published in: Prenatal Diagnosis

date of publication: 2001-03-01

main subject: myotonic dystrophy

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Cites articles 21

Date

Title

Authors

1975-07-01

Congenital myotonic dystrophy in Britain. II. Genetic basis
1985-01-01

The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus
1989-12-01

Presymptomatic detection and prenatal diagnosis for myotonic dystrophy by means of linked DNA markers
1989-07-01

Myotonic dystrophy: developments in molecular genetics
1991-02-01

Prenatal diagnosis of myotonic dystrophy using closely linked flanking markers
1992-02-01

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member
1992-03-01

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene
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Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy
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Diagnosis of Down syndrome and other aneuploidies using quantitative polymerase chain reaction and small tandem repeat polymorphisms
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Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring
1993-12-01

Genomic organization and transcriptional units at the myotonic dystrophy locus
1997-06-01

Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patients.
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A technique for eliminating allele specific amplification failure during DNA amplification of heterozygous cells for preimplantation diagnosis
1997-10-01

Clinical application of preimplantation diagnosis for myotonic dystrophy

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1997-04-01

Prenatal detection of fetal aneuploidies using transcervical cell samples
1998-03-01

Preimplantation genetic diagnosis of inherited cancer: familial adenomatous polyposis coli
1998-08-01

Fluorescent PCR and automated fragment analysis for the clinical application of preimplantation genetic diagnosis of myotonic dystrophy (Steinert's disease)

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Preimplantation diagnosis for Huntington's disease (HD): clinical application and analysis of the HD expansion in affected embryos

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Assessment of diagnostic quantitative fluorescent multiplex polymerase chain reaction assays performed on single cells

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