(Q47715684)

English

An explanation of the apparently increased incidence of moderate mental retardation in Turner's syndrome

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4715982

An explanation of the apparently increased incidence of moderate mental retardation in Turner's syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4715982

moderate mental retardation

1 reference

based on heuristic

inferred from title

author name string

D C Garron

1

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4715982

L Molander

2

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4715982

B Cronholm

3

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4715982

J Lindsten

4

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4715982

language of work or name

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publication date

1 March 1973

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4715982

Behavior Genetics

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4715982

3

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4715982

1

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4715982

37-43

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4715982

https://scigraph.springernature.com/pub.10.1007/bf01067687

0 references

TWO CYTOGENETIC SYNDROMES: PSYCHOLOGIC COMPARISONS. I. INTELLIGENCE AND SPECIFIC-FACTOR QUOTIENTS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4715982

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of personality pathology in Turner's syndrome: Relation to cytogenetics, hormones and physique

1 reference

https://pubmed.ncbi.nlm.nih.gov/4715982

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex-linked, recessive inheritance of spatial and numerical abilities, and Turner's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4715982

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mental retardation and cognitive defects in XO-Turner's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4715982

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic and psychosexual incongruities with a note on space-form blindness

1 reference

https://pubmed.ncbi.nlm.nih.gov/4715982

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A factor-analytically based rationale for the Wechsler Adult Intelligence Scale

1 reference

https://pubmed.ncbi.nlm.nih.gov/4715982

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A specific cognitive deficit observed in gonadal aplasia (Turner's syndrome).

1 reference

https://pubmed.ncbi.nlm.nih.gov/4715982

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Personality and intelligence in Turner's syndrome. A critical review

1 reference

https://pubmed.ncbi.nlm.nih.gov/4715982

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IQ and the somatic stigmata of Turner's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4715982

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01067687

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4715982

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4715982

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