(Q50306237)

http://europepmc.org/abstract/MED/24963073

2 March 2018

title

Mutational analyses of the FMR1 gene in Chinese pediatric population of fragile x suspects: low tolerance for point mutation. (English)

1 reference

http://europepmc.org/abstract/MED/24963073

2 March 2018

author

Shiyu Luo

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24963073%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

author name string

Wen Huang

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24963073%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Qiuping Xia

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24963073%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Qian Du

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24963073%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Lingqian Wu

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24963073%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Ranhui Duan

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24963073%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

publication date

23 June 2014

1 reference

http://europepmc.org/abstract/MED/24963073

2 March 2018

published in

Journal of Child Neurology

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24963073%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

volume

30

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24963073%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24963073%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

page(s)

803-806

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24963073%20AND%20SRC:MED&resulttype=core&format=json

Fragile X and autism: Intertwined at the molecular level leading to targeted treatments

10 June 2020

cites work

1 reference

https://api.crossref.org/works/10.1177%2F0883073814538508

Mutation spectra in fragile X syndrome induced by deletions of CGG*CCG repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073814538508

A point mutation in the FMR-1 gene associated with fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073814538508

A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073814538508

Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073814538508

A nonsense mutation in FMR1 causing fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073814538508

Single-strand conformation polymorphism analysis of the FMR1 gene in autistic and mentally retarded children in Japan.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073814538508

21 January 2018

Identifiers

DOI

10.1177/0883073814538508

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24963073%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

1 reference