Identification of the gene FMR2, associated with FRAXE mental retardation (Q34385889)

1 August 2017

Identification of the gene FMR2, associated with FRAXE mental retardation (English)

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1 August 2017

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1 August 2017

Gedeon AK

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1 August 2017

Sutherland GR

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3

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1 August 2017

Mulley JC

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4

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1 August 2017

language of work or name

English

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publication date

1 May 1996

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1 August 2017

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1 August 2017

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1 August 2017

105-108

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https://scigraph.springernature.com/pub.10.1038/ng0596-105

1 August 2017

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cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

Basic local alignment search tool

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

The proline-rich transcriptional activator of CTF/NF-I is distinct from the replication and DNA binding domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

Fragile X genotype characterized by an unstable region of DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

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

https://api.crossref.org/works/10.1038%2FNG0596-105

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

7 January 2021

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

7 January 2021

Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis.

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

7 January 2021

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

7 January 2021

Characterisation of a new rare fragile site easily confused with the fragile X

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

7 January 2021

FRAXE and mental retardation

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

7 January 2021

Human genes containing polymorphic trinucleotide repeats

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

7 January 2021

Genes on chromosomes 4, 9, and 19 involved in 11q23 abnormalities in acute leukemia share sequence homology and/or common motifs

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

7 January 2021

How many X-linked genes for non-specific mental retardation (MRX) are there?

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

7 January 2021

Molecular cloning of the human esterase D gene, a genetic marker of retinoblastoma

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-105

7 January 2021

Identifiers

DOI

10.1038/NG0596-105

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Dimensions Publication ID

1 August 2017

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