(Q24538769)

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

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Europe PubMed Central

PubMed publication ID

5 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

language disorder

1 reference

based on heuristic

inferred from title

2

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Europe PubMed Central

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5 July 2017

12

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Europe PubMed Central

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5 July 2017

Faraneh Vargha-Khadem

11

object named as

F Vargha-Khadem

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Europe PubMed Central

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5 July 2017

author name string

C S Lai

1

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Europe PubMed Central

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5 July 2017

J A Hurst

3

1 reference

Europe PubMed Central

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5 July 2017

E R Levy

4

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Europe PubMed Central

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5 July 2017

S Hodgson

5

1 reference

Europe PubMed Central

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5 July 2017

M Fox

6

1 reference

Europe PubMed Central

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5 July 2017

S Jeremiah

7

1 reference

Europe PubMed Central

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5 July 2017

S Povey

8

1 reference

Europe PubMed Central

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5 July 2017

D C Jamison

9

1 reference

Europe PubMed Central

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5 July 2017

E D Green

10

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Europe PubMed Central

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5 July 2017

language of work or name

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publication date

5 July 2000

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Europe PubMed Central

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5 July 2017

American Journal of Human Genetics

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Europe PubMed Central

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5 July 2017

67

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Europe PubMed Central

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5 July 2017

2

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Europe PubMed Central

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5 July 2017

357-368

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

Neural basis of an inherited speech and language disorder.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

24 March 2017

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

24 March 2017

Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

24 March 2017

cDNAs with long CAG trinucleotide repeats from human brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

24 March 2017

An autosomal genomic screen for autism. Collaborative linkage study of autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

24 March 2017

Genetic studies of autistic disorder and chromosome 7

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

24 March 2017

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

24 March 2017

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

24 March 2017

Localisation of a gene implicated in a severe speech and language disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

24 March 2017

A Gene Map of the Human Genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

24 March 2017

An extended family with a dominantly inherited speech disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

24 March 2017

Feature-blind grammar and dysphagia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

24 March 2017

A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kb.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

27 September 2017

IRE-bubble PCR: a rapid method for efficient and representative amplification of human genomic DNA sequences from complex sources

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

27 September 2017

Familial aggregation of a developmental language disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

27 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

29 November 2018

A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

29 November 2018

A gene-based genetic linkage and comparative map of the rat X chromosome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

29 November 2018

Genetic basis of specific language impairment: evidence from a twin study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287211

29 November 2018

Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/10880297

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Position effect in human genetic disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/10880297

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Speech and language defects

1 reference

https://api.crossref.org/works/10.1086%2F303011

7 January 2021

based on heuristic

inferred from DOI database lookup

Genome maps 7. The human transcript map. Wall chart

1 reference

https://api.crossref.org/works/10.1086%2F303011

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

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Europe PubMed Central

PubMed publication ID

5 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

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