(Q43108911)

English

Using genetics to dissect cognition

scientific article published in January 1997

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

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Using genetics to dissect cognition (English)

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

author name string

Pennington BF

1

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

language of work or name

0 references

publication date

1 January 1997

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

60

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

1

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

13-16

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712539

25 May 2018

Quantitative trait locus for reading disability on chromosome 6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712539

25 May 2018

Genetics of learning disabilities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712539

25 May 2018

Perception of the speech code

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712539

25 May 2018

Phonological processing skills and deficits in adult dyslexics.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712539

25 May 2018

Specific reading disability: identification of an inherited form through linkage analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8981941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specific dyslexia (congenital word-blindness); a clinical and genetic study

1 reference

https://pubmed.ncbi.nlm.nih.gov/8981941

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

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