(Q41141324)

27 September 2017

title

A controlled study of longitudinal IQ changes in females and males with fragile X syndrome (English)

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27 September 2017

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Wright-Talamante C

1

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27 September 2017

Cheema A

2

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27 September 2017

Riddle JE

3

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27 September 2017

Luckey DW

4

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27 September 2017

Taylor AK

5

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27 September 2017

Hagerman RJ

6

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27 September 2017

publication date

1 August 1996

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American Journal of Medical Genetics Part A

27 September 2017

published in

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27 September 2017

volume

64

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27 September 2017

issue

2

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27 September 2017

page(s)

350-355

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Molecular-neurobehavioral associations in females with the fragile X full mutation.

27 September 2017

cites work

1 reference

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Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype

21 January 2018

1 reference

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The trajectory of cognitive development in males with fragile X syndrome

21 January 2018

1 reference

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Trajectory of adaptive behavior in males with fragile X syndrome.

21 January 2018

1 reference

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Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960809%2964%3A2%3C350%3A%3AAID-AJMG23%3E3.0.CO%3B2-D

High functioning fragile X males: demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression

21 January 2018

1 reference

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Does IQ decline with age in fragile-X? A methodological critique

21 January 2018

1 reference

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Developmental implications of changing trajectories of IQ in males with fragile X syndrome.

21 January 2018

1 reference

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Fragile X syndrome in a normal IQ male with learning and emotional problems.

21 January 2018

1 reference

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Neuroanatomy of fragile X syndrome: the temporal lobe

21 January 2018

1 reference

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Neurodevelopmental effects of the FMR-1 full mutation in humans.

21 January 2018

1 reference

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Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

21 January 2018

1 reference

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Normal phenotype in two brothers with a full FMR1 mutation.

21 January 2018

1 reference

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Rapid antibody test for fragile X syndrome.

21 January 2018

1 reference

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Longitudinal changes in IQ among fragile X females: a preliminary multicenter analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960809%2964%3A2%3C350%3A%3AAID-AJMG23%3E3.0.CO%3B2-D

Longitudinal IQ changes in fragile X males

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960809%2964%3A2%3C350%3A%3AAID-AJMG23%3E3.0.CO%3B2-D

10.1002/(SICI)1096-8628(19960809)64:2<350::AID-AJMG23>3.0.CO;2-D

21 January 2018

Identifiers

DOI

1 reference

27 September 2017

1 reference