(Q34561421)

3 August 2017

1 reference

title

Different approaches to relating genotype to phenotype in developmental disorders (English)

1 reference

3 August 2017

1 reference

2

Gaia Scerif

0 references

Annette Karmiloff-Smith

series ordinal

1

object named as

Annette Karmiloff-Smith

1 reference

3 August 2017

Michael Thomas

3

0 references

author name string

Gaia Scerif

series ordinal

2

1 reference

3 August 2017

1 April 2002

1 reference

Developmental Psychobiology

3 August 2017

1 reference

3 August 2017

40

1 reference

3 August 2017

3

1 reference

3 August 2017

311-322

1 reference

Variability in FMRP and early development in males with fragile X syndrome.

3 August 2017

1 reference

Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome

21 January 2018

1 reference

Population and familial association between the D4 dopamine receptor gene and measures of Novelty Seeking

21 January 2018

1 reference

Fragile X mice develop sensory hyperreactivity to auditory stimuli

21 January 2018

1 reference

Syntax and morphology in Williams syndrome.

21 January 2018

1 reference

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

21 January 2018

1 reference

Differential impact of the FMR-1 full mutation on memory and attention functioning : a neuropsychological perspective.

21 January 2018

1 reference

Genetics of mouse behavior: interactions with laboratory environment.

21 January 2018

1 reference

Prenatal development of monozygotic twins and concordance for schizophrenia

21 January 2018

1 reference

Configural and local processing of faces in children with Williams syndrome.

21 January 2018

1 reference

Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group

21 January 2018

1 reference

The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

21 January 2018

1 reference

Fmr1 knockout mouse has a distinctive strain-specific learning impairment.

21 January 2018

1 reference

Williams syndrome: from genotype through to the cognitive phenotype

21 January 2018

1 reference

Annotation: behavioural phenotypes: a window onto the biology of behaviour

21 January 2018

1 reference

Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes.

21 January 2018

1 reference

Cognitive profiles associated with the fra(X) syndrome in males and females.

21 January 2018

1 reference

Synaptic regulation of protein synthesis and the fragile X protein

21 January 2018

1 reference

Disordered visual processing and oscillatory brain activity in autism and Williams syndrome.

21 January 2018

1 reference

Analysis of mammalian central nervous system gene expression and function using bacterial artificial chromosome-mediated transgenesis

21 January 2018

1 reference

Towards new models of disease and physiology in the neurosciences: the role of induced and naturally occurring mutations

21 January 2018

1 reference

Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination.

21 January 2018

1 reference

Understanding the molecular basis of fragile X syndrome

21 January 2018

1 reference

Development itself is the key to understanding developmental disorders

21 January 2018

1 reference

Language and Williams syndrome: how intact is "intact"?

21 January 2018

1 reference

More hippocampal neurons in adult mice living in an enriched environment

21 January 2018

1 reference

An evaluation of what the mouse knockout experiments are telling us about mammalian behaviour

21 January 2018

1 reference

Functional brain activation during cognition is related to FMR1 gene expression.

21 January 2018

1 reference

III. Electrophysiological studies of face processing in Williams syndrome

21 January 2018

1 reference

A neuropsychological profile of attention deficits in young males with fragile X syndrome.

21 January 2018

1 reference

Cognitive modularity and genetic disorders.

21 January 2018

1 reference

Psychosocial influences: Critiques, findings, and research needs

21 January 2018

1 reference

Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis

21 January 2018

1 reference

Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes

21 January 2018

1 reference

A cognitive and behavioural phenotype in williams syndrome

21 January 2018

1 reference

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

Glutamate receptors and development of the visual cortex: effect of metabotropic agonists on cAMP

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/DEV.10035

1 reference

3 August 2017

1 reference

PubMed ID

11891641