(Q30470934)

English

Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families (English)

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Stephen Petrill

6

object named as

Stephen A Petrill

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Europe PubMed Central

PMC publication ID

19 October 2017

author name string

Tabatha R Simmons

1

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Europe PubMed Central

PMC publication ID

19 October 2017

Judy F Flax

2

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Marco A Azaro

3

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Jared E Hayter

4

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Laura M Justice

5

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Anne S Bassett

7

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Paula Tallal

8

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Linda M Brzustowicz

9

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Europe PubMed Central

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19 October 2017

Christopher W Bartlett

10

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Europe PubMed Central

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19 October 2017

publication date

14 October 2010

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Europe PubMed Central

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19 October 2017

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Europe PubMed Central

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19 October 2017

70

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Europe PubMed Central

PMC publication ID

19 October 2017

4

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

232-244

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Europe PubMed Central

PMC publication ID

19 October 2017

describes a project that uses

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Europe PubMed Central

18 June 2022

https://europepmc.org/article/PMC/3085518

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inferred from PubMed Central ID database lookup

CMIP and ATP2C2 modulate phonological short-term memory in language impairment

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

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Improving language and literacy is a matter of time

1 reference

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Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment

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1 reference

https://pubmed.ncbi.nlm.nih.gov/20948219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/20948219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/20948219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial aggregation in specific language impairment

1 reference

https://pubmed.ncbi.nlm.nih.gov/20948219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is preschool language impairment a risk factor for dyslexia in adolescence?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20948219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accumulating quantitative trait linkage evidence across multiple datasets using the posterior probability of linkage

1 reference

https://pubmed.ncbi.nlm.nih.gov/20948219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A New Method for Computing the Multipoint Posterior Probability of Linkage

1 reference

https://pubmed.ncbi.nlm.nih.gov/20948219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1159/000320367

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

ResearchGate publication ID

0 references

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