Heritable unstable DNA sequences (Q67482165)

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13 September 2019

title

Heritable unstable DNA sequences (English)

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13 September 2019

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10 September 2022

Richards RI

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13 September 2019

Sutherland GR

series ordinal

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13 September 2019

language of work or name

English

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National Center for Biotechnology Information

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10 September 2022

publication date

1 April 1992

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13 September 2019

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13 September 2019

volume

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13 September 2019

issue

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13 September 2019

page(s)

7-9

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Hereditary unstable DNA: a new explanation for some old genetic questions?

13 September 2019

cites work

1 reference

7 January 2021

Fragile X genotype characterized by an unstable region of DNA.

1 reference

7 January 2021

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

7 January 2021

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

1 reference

7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

7 January 2021

Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island

1 reference

7 January 2021

Prenatal diagnosis of fragile X syndrome by direct detection of the unstable DNA sequence

1 reference

7 January 2021

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

7 January 2021

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

1 reference

7 January 2021

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

1 reference

7 January 2021

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

1 reference

7 January 2021

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

1 reference

7 January 2021

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

1 reference

7 January 2021

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

1 reference

7 January 2021

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

1 reference

7 January 2021

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

1 reference

7 January 2021

Absence of expression of the FMR-1 gene in fragile X syndrome

1 reference

7 January 2021

Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms

1 reference

7 January 2021

The use of synthetic tandem repeats to isolate new VNTR loci: cloning of a human hypermutable sequence

1 reference

7 January 2021

Unique organization of the human BCR gene promoter

1 reference

7 January 2021

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site

1 reference

7 January 2021

Slippage synthesis of simple sequence DNA

1 reference

7 January 2021

Positional cloning: let's not call it reverse anymore

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG0492-7

1 reference

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13 September 2019

1 reference

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