(Q33971586)

30 July 2017

1 reference

title

Advances in research on the fragile X syndrome (English)

1 reference

30 July 2017

1 reference

Mazzocco MM

1

1 reference

30 July 2017

publication date

1 January 2000

1 reference

Mental Retardation and Developmental Disabilities Research Reviews

30 July 2017

published in

1 reference

30 July 2017

volume

6

1 reference

30 July 2017

issue

2

1 reference

30 July 2017

page(s)

96-106

1 reference

Cognitive, behavioral, and neuroanatomical assessment of two unrelated male children expressing FRAXE.

30 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

FMR1 protein: conserved RNP family domains and selective RNA binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Examination of factors associated with instability of the FMR1 CGG repeat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Early developmental trajectories of males with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Autistic behavior in young boys with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

A candidate gene for mild mental handicap at the FRAXE fragile site

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Spatial cognition in males with Fragile-X syndrome: evidence for a neuropsychological phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

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/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Screening with the FMR1 protein test among mentally retarded males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

The trajectory of cognitive development in males with fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Trajectory of adaptive behavior in males with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Quantitative comparison of FMR1 gene expression in normal and premutation alleles

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

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/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Molecular evidence that fragile X syndrome occurs in the South African black population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

A de novo deletion in FMR1 in a patient with developmental delay

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Evaluation of school children at high risk for fragile X syndrome utilizing buccal cell FMR-1 testing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Behavioral style of young boys with fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Analysis of neocortex in three males with the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Two new cases of FMR1 deletion associated with mental impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Molecular and cellular genetics of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Fragile X premutations are not a major cause of early menopause

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Characterization of the full fragile X syndrome mutation in fetal gametes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Social functioning among girls with fragile X or Turner syndrome and their sisters

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Specific frontal lobe deficits among women with the fragile X gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Autistic behaviors among girls with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

The prevalence of the FMR1 and FMR2 mutations among preschool children with language delay

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Brief report: autistic behaviors among children with fragile X or Rett syndrome: implications for the classification of pervasive developmental disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

An n-allele model for progressive amplification in the FMR1 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Contribution of the FMR1 gene mutation to human intellectual dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Postmortem examination of two fragile X brothers with an FMR1 full mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Arithmetic disabilities, specific and otherwise: a neuropsychological perspective.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

No mental retardation in a man with 40% abnormal methylation at the FMR-1 locus and transmission of sperm cell mutations as premutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Obstetrical and gynecological complications in fragile X carriers: a multicenter study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

High proportion of twins in carriers of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream region.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Dizygous twinning and premature menopause in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Family contexts, parental behaviour, and personality profiles of children and adolescents with Prader-Willi, fragile-X, or Williams syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

FRAXA locus in fragile X diagnosis: family studies, prenatal diagnosis, and diagnosis of sporadic cases of mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Synaptic synthesis of the Fragile X protein: possible involvement in synapse maturation and elimination

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Efficacy of cascade testing for fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Mitotic stability of fragile X mutations in differentiated cells indicates early post-conceptional trinucleotide repeat expansion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Fragile X genotype characterized by an unstable region of DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Reduced mRNA for G3BP in fragile X cells: evidence of FMR1 gene regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1098-2779%282000%296%3A2%3C96%3A%3AAID-MRDD3%3E3.0.CO%3B2-H

10.1002/1098-2779(2000)6:2<96::AID-MRDD3>3.0.CO;2-H

21 January 2018

Identifiers

DOI

1 reference

30 July 2017

1 reference