scholarly article | Q13442814 |
P50 | author | Robert Plomin | Q3401334 |
P2093 | author name string | I W Craig | |
C S Loat | |||
G Craig | |||
P2860 | cites work | Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation | Q24533431 |
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The fragile X mental retardation protein inhibits translation via interacting with mRNA | Q28588486 | ||
Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome | Q29616495 | ||
Twins early development study (TEDS): a multivariate, longitudinal genetic investigation of language, cognition and behavior problems in childhood | Q30882486 | ||
Aging in individuals with the FMR1 mutation | Q30909849 | ||
Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS). | Q30988960 | ||
A high density of X-linked genes for general cognitive ability: a run-away process shaping human evolution? | Q34102797 | ||
A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation | Q34199966 | ||
The (CGG)n repeat element within the 5' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter | Q34266389 | ||
Premature ovarian failure in the fragile X syndrome | Q34306135 | ||
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Fragile X mental retardation protein is associated with translating polyribosomes in neuronal cells. | Q40524276 | ||
Variability in early communicative development | Q40585574 | ||
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Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. | Q46666276 | ||
RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila | Q47071910 | ||
Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles | Q47192550 | ||
FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy | Q50279964 | ||
FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure. | Q51927334 | ||
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Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers. | Q51965229 | ||
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DNA by mail: an inexpensive and noninvasive method for collecting DNA samples from widely dispersed populations. | Q52194659 | ||
Prenatal diagnosis and carrier screening for fragile X by PCR. | Q52200609 | ||
Genetics, genes, genomics and g | Q56268245 | ||
X-linked mental retardation | Q56270643 | ||
Telephone Testing and Teacher Assessment of Reading Skills in 7-year-olds: I. Substantial Correspondence for a Sample of 5544 Children and for Extremes | Q57278071 | ||
A Twin Study of Teacher-Reported Mathematics Performance and Low Performance in 7-Year-Olds | Q57278074 | ||
Phenotypic g early in life | Q57278087 | ||
Testing cognitive abilities by telephone in a sample of 6- to 8-year-olds | Q57278095 | ||
DNA from buccal swabs recruited by mail: evaluation of storage effects on long-term stability and suitability for multiplex polymerase chain reaction genotyping | Q57949031 | ||
P433 | issue | Pt 5 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 555-565 | |
P577 | publication date | 2006-09-01 | |
P1433 | published in | Annals of Human Genetics | Q4767852 |
P1476 | title | Investigating the relationship between FMR1 allele length and cognitive ability in children: a subtle effect of the normal allele range on the normal ability range? | |
P478 | volume | 70 |
Q51926110 | Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: preliminary data suggest an involvement of epigenetic mechanisms. |
Q34984624 | Motor deficits on a ladder rung task in male and female adolescent and adult CGG knock-in mice |
Q54375474 | Neuregulin 1-induced AKT and ERK phosphorylation in patients with fragile X syndrome (FXS) and intellectual disability associated with obstetric complications. |