(Q50278621)

28 February 2018

title

An investigation of FRAXA intermediate allele phenotype in a longitudinal sample. (English)

1 reference

28 February 2018

author

Anna Murray

2

1 reference

28 February 2018

Newton Ennis Morton

8

object named as

N E Morton

1 reference

28 February 2018

S Ennis

1

1 reference

28 February 2018

S Youings

3

1 reference

28 February 2018

G Brightwell

4

1 reference

28 February 2018

D Herrick

5

1 reference

28 February 2018

S Ring

6

1 reference

28 February 2018

M Pembrey

7

1 reference

28 February 2018

P A Jacobs

9

1 reference

28 February 2018

language of work or name

English

0 references

publication date

1 March 2006

1 reference

28 February 2018

published in

Annals of Human Genetics

1 reference

28 February 2018

volume

70

1 reference

28 February 2018

issue

Pt 2

1 reference

28 February 2018

page(s)

170-180

1 reference

28 February 2018

Autistic behavior in young boys with fragile X syndrome.

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

ALSPAC--the Avon Longitudinal Study of Parents and Children. I. Study methodology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

A new human genetic resource: a DNA bank established as part of the Avon longitudinal study of pregnancy and childhood (ALSPAC).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

Reproductive and menstrual history of females with fragile X expansions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

Cognitive and behavioral performance among FMR1 high-repeat allele carriers surveyed from special education classes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

FRAXA and FRAXE: evidence against segregation distortion and for an effect of intermediate alleles on learning disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

FRAXA and FRAXE: the results of a five year survey

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1529-8817.2005.00220.X

10.1111/J.1529-8817.2005.00220.X

21 January 2018

Identifiers

DOI

1 reference

28 February 2018

PubMed ID

16626328

1 reference

28 February 2018