(Q40727124)

23 September 2017

title

Behavior phenotype of FG syndrome: cognition, personality, and behavior in eleven affected boys (English)

1 reference

23 September 2017

1 reference

Ozonoff S

1

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23 September 2017

Williams BJ

series ordinal

2

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23 September 2017

Rauch AM

series ordinal

3

1 reference

23 September 2017

Opitz JO

series ordinal

4

1 reference

23 September 2017

publication date

1 January 2000

1 reference

American Journal of Medical Genetics Part A

23 September 2017

published in

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23 September 2017

volume

97

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23 September 2017

issue

2

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23 September 2017

page(s)

112-118

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Autism screening questionnaire: diagnostic validity.

23 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200022%2997%3A2%3C112%3A%3AAID-AJMG2%3E3.0.CO%3B2-D

Tower of Hanoi performance of retarded young adults and nonretarded children as a function of solution length and goal state.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200022%2997%3A2%3C112%3A%3AAID-AJMG2%3E3.0.CO%3B2-D

Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200022%2997%3A2%3C112%3A%3AAID-AJMG2%3E3.0.CO%3B2-D

The "little five": exploring the nomological network of the five-factor model of personality in adolescent boys

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200022%2997%3A2%3C112%3A%3AAID-AJMG2%3E3.0.CO%3B2-D

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200022%2997%3A2%3C112%3A%3AAID-AJMG2%3E3.0.CO%3B2-D

Language and development in FG syndrome with callosal agenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200022%2997%3A2%3C112%3A%3AAID-AJMG2%3E3.0.CO%3B2-D

Studies of malformation syndromes of man XXXIII: The FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200022%2997%3A2%3C112%3A%3AAID-AJMG2%3E3.0.CO%3B2-D

FG syndrome update 1988: note of 5 new patients and bibliography

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200022%2997%3A2%3C112%3A%3AAID-AJMG2%3E3.0.CO%3B2-D

Executive functions and developmental psychopathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200022%2997%3A2%3C112%3A%3AAID-AJMG2%3E3.0.CO%3B2-D

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200022%2997%3A2%3C112%3A%3AAID-AJMG2%3E3.0.CO%3B2-D

A gene for FG syndrome maps in the Xq12-q21.31 region

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200022%2997%3A2%3C112%3A%3AAID-AJMG2%3E3.0.CO%3B2-D

Clinical and behavioral characteristics in FG syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200022%2997%3A2%3C112%3A%3AAID-AJMG2%3E3.0.CO%3B2-D

2-year-old boy who has been diagnosed with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200022%2997%3A2%3C112%3A%3AAID-AJMG2%3E3.0.CO%3B2-D

10.1002/1096-8628(200022)97:2<112::AID-AJMG2>3.0.CO;2-D

21 January 2018

Identifiers

DOI

1 reference

23 September 2017

1 reference