(Q58443310)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22740120%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

title

Filamin A mutation associated with normal reading skills and dyslexia in a family with periventricular heterotopia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22740120%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

1 reference

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22740120%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

4

David L Rimoin

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22740120%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

1

Eyal Reinstein

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22740120%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

author name string

Tami Katzir

series ordinal

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22740120%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Bernard S Chang

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22740120%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

language of work or name

English

0 references

publication date

27 June 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22740120%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics

6 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22740120%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

volume

158A

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22740120%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22740120%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

page(s)

1897-1901

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22740120%20AND%20SRC:MED&resulttype=core&format=json

Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci

6 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35455

A structural basis for reading fluency: white matter defects in a genetic brain malformation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35455

Genetic and environmental influences on orthographic and phonological skills in children with reading disabilities

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35455

Genetic and environmental influences on individual differences in printed word recognition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35455

Commingling and segregation analysis of reading performance in families of normal reading probands.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35455

The varieties of pathways to dysfluent reading: comparing subtypes of children with dyslexia at letter, word, and connected text levels of reading

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35455

Like father, like son: periventricular nodular heterotopia and nonverbal learning disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35455

White matter microstructural differences linked to left perisylvian language network in children with dyslexia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35455

Filamin A: phenotypic diversity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35455

In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35455

Specific disorders and broader phenotypes: the case of dyslexia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35455

Gray matter volumes and cognitive ability in the epileptogenic brain malformation of periventricular nodular heterotopia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35455

Family patterns of developmental dyslexia: clinical findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35455

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.35455

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22740120%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

1 reference