FRA2A is a CGG repeat expansion associated with silencing of AFF3 (Q35156954)

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15 March 2020

title

FRA2A is a CGG repeat expansion associated with silencing of AFF3 (English)

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15 March 2020

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15 March 2020

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15 March 2020

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15 March 2020

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15 March 2020

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15 March 2020

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15 March 2020

Sofie Metsu

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15 March 2020

Liesbeth Rooms

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15 March 2020

Jacqueline Rainger

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15 March 2020

Hemant Bengani

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15 March 2020

Chandra Sekhar Reddy Chilamakuri

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15 March 2020

Harris Morrison

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15 March 2020

Edwin Reyniers

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15 March 2020

Evelyn Douglas

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15 March 2020

Geoffrey Thompson

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15 March 2020

Eric Haan

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15 March 2020

publication date

24 April 2014

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15 March 2020

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15 March 2020

volume

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15 March 2020

issue

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15 March 2020

page(s)

e1004242

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Creative Commons Attribution 4.0 International

15 March 2020

start time

24 April 2014

1 reference

April 2022 Public Data File from Crossref

copyrighted

0 references

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13 July 2018

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13 July 2018

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13 July 2018

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13 July 2018

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13 July 2018

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13 July 2018

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13 July 2018

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13 July 2018

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13 July 2018

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Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH.

13 July 2018

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Developmental stages in human embryos: revised and new measurements

27 September 2018

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The molecular basis of the folate-sensitive fragile site FRA11A at 11q13.

27 September 2018

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Evolutionary breakpoints are co-localized with fragile sites and intrachromosomal telomeric sequences in primates.

27 September 2018

1 reference

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Timing of the absence of FMR1 expression in full mutation chorionic villi

27 September 2018

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The mouse Laf4 gene: exon/intron organization, cDNA sequence, alternative splicing, and expression during central nervous system development.

27 September 2018

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Mental retardation with rare fragile site expressed at 2q11.

27 September 2018

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Clinical and genetic implications of dynamic mutations in neuropediatric practice

27 September 2018

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

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3998887

A fragile secondary constriction on chromosome 2 in five patients with different clinical features

27 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24763282

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24763282

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

DNA methylation analysis by pyrosequencing

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24763282

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1004242

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24763282%20AND%20SRC:MED&resulttype=core&format=json

15 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24763282%20AND%20SRC:MED&resulttype=core&format=json

15 March 2020

PubMed publication ID

24763282

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24763282%20AND%20SRC:MED&resulttype=core&format=json