(Q24672211)

developmental verbal dyspraxia

inferred from title

1 reference

21

0 references

Katariina Hannula-Jouppi

23

Katariina Hannula-Jouppi

0 references

Marita Lipsanen-Nyman

3

Marita Lipsanen-Nyman

0 references

A. Micheil Innes

Micheil Innes

8

0 references

Peter Szatmari

15

Peter Szatmari

0 references

Stephen W. Scherer

22

Stephen W Scherer

0 references

Janis Oram Cardy

Janis Oram Cardy

20

0 references

Anne O. Summers

14

Anne Summers

0 references

Wendy Roberts

12

Wendy Roberts

0 references

Lars Feuk

1

Lars Feuk

0 references

Jennifer Skaug

4

Jennifer Skaug

0 references

Lili Senman

13

Lili Senman

0 references

Susan Zeesman

18

Susan Zeesman

0 references

author name string

Aino Kalervo

2

0 references

Marita Lipsanen-Nyman

3

0 references

Kazuhiko Nakabayashi

5

0 references

Brenda Finucane

6

0 references

Danielle Hartung

7

0 references

Batsheva Kerem

9

0 references

Malgorzata J Nowaczyk

10

0 references

Joseph Rivlin

11

0 references

Virginia Wong

16

0 references

John B Vincent

17

0 references

Lucy R Osborne

19

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Katariina Hannula-Jouppi

American Journal of Human Genetics

23

0 references

language of work or name

English

0 references

publication date

November 2006

0 references

published in

0 references

volume

79

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issue

5

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page(s)

965-72

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cites work

Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Human chromosome 7: DNA sequence and biology

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

FOXP2 is not a major susceptibility gene for autism or specific language impairment

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Molecular evolution of FOXP2, a gene involved in speech and language

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Detection of large-scale variation in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

FOXP2 and the neuroanatomy of speech and language

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

A forkhead-domain gene is mutated in a severe speech and language disorder

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Genetic studies of autistic disorder and chromosome 7

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

An extended family with a dominantly inherited speech disorder

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Fox's in development and disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Association of specific language impairment (SLI) to the region of 7q31.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

FOXP2: novel exons, splice variants, and CAG repeat length stability

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Evaluation of FOXP2 as an autism susceptibility gene

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Phenotypic variability in Angelman syndrome: comparison among different deletion classes and between deletion and UPD subjects.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype?

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile cilia

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1698557

Genetic Screening for Maternal Uniparental Disomy of Chromosome 7 in Prenatal and Postnatal Growth Retardation of Unknown Cause

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17033973

12 December 2020

inferred from PubMed ID database lookup

Parental origin of de novo chromosome rearrangements

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17033973

12 December 2020

inferred from PubMed ID database lookup

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17033973

12 December 2020

inferred from PubMed ID database lookup

Molecular Cytogenetics of Autism

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F508902

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/508902

1 reference

1 reference

1 reference

PubMed publication ID

17033973

1 reference