(Q71350608)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7425998%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

title

Genetic models of reading disability (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7425998%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

1 reference

F I Lewitter

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7425998%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

J C DeFries

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7425998%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

R C Elston

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7425998%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

publication date

1 January 1980

1 reference

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18 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7425998%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

volume

10

1 reference

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18 October 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7425998%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

page(s)

9-30

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf01067316

18 October 2019

exact match

0 references

cites work

Study of the genetic transmission of hypercholesterolemia and hypertriglyceridemia in a 195 member kindred

1 reference

12 December 2020

A General Model for the Genetic Analysis of Pedigree Data

1 reference

12 December 2020

Genetics of common disorders

1 reference

12 December 2020

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

1 reference

12 December 2020

Studies on blood and urine glucose in Seminole Indians: indications for segregation of a major gene

1 reference

12 December 2020

The genetics of specific reading disability

1 reference

12 December 2020

Segregation analysis in human genetics

1 reference

12 December 2020

A genetic study of schizophrenia pedigrees. II. One-locus hypotheses

1 reference

12 December 2020

Analysis of family resemblance. IV. Operational characteristics of segregation analysis

1 reference

12 December 2020

A Case of Congenital Word Blindness

1 reference

12 December 2020

LATERAL DOMINANCE, LATERAL AWARENESS, AND READING DISABILITY

1 reference

12 December 2020

Efficiency and robustness of pedigree segregation analysis

1 reference

12 December 2020

Reading disability in twins

1 reference

12 December 2020

Genetical investigations in dyslexia

1 reference

12 December 2020

General models for segregation analysis

1 reference

12 December 2020

Familial Nature of Reading Disability

1 reference

12 December 2020

Sampling considerations in the gathering and analysis of pedigree data

1 reference

12 December 2020

Is congenital word-blindness a hereditary type of Gerstmann's syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01067316

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7425998%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

1 reference