(Q37324277)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19074489%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

title

Trajectories and predictors of the development of very young boys with fragile X syndrome (English)

1 reference

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18 January 2020

1 reference

7

1 reference

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18 January 2020

author name string

Jane E Roberts

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19074489%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Jean B Mankowski

2

1 reference

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18 January 2020

John Sideris

3

1 reference

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18 January 2020

Barbara Davis Goldman

4

1 reference

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18 January 2020

Deborah D Hatton

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19074489%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Penny L Mirrett

6

1 reference

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18 January 2020

J Steven Reznick

8

1 reference

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18 January 2020

Anna C J Long

9

1 reference

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18 January 2020

Donald B Bailey

10

1 reference

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18 January 2020

language of work or name

1 reference

12 December 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19074489%20AND%20SRC:MED&resulttype=core&format=json

Journal of Pediatric Psychology

18 January 2020

published in

1 reference

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18 January 2020

volume

34

1 reference

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18 January 2020

issue

8

1 reference

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18 January 2020

page(s)

827-836

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19074489%20AND%20SRC:MED&resulttype=core&format=json

Analysis of clinical features predicting etiologic yield in the assessment of global developmental delay

18 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Fragile X syndrome: an update and review for the primary pediatrician

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Detecting and addressing developmental and behavioral problems in primary care.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

FMR1 and the fragile X syndrome: human genome epidemiology review

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Co-occurring conditions associated with FMR1 gene variations: findings from a national parent survey.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Risk of cognitive impairment in female premutation carriers of fragile X premutation: analysis by means of robust segmented linear regression models.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Mood and anxiety disorders in females with the FMR1 premutation

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Early temperament and negative reactivity in boys with fragile X syndrome.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Developmental trajectories and correlates of sensory processing in young boys with fragile X syndrome.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Child and genetic variables associated with maternal adaptation to fragile X syndrome: a multidimensional analysis.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Identifying infants and young children with developmental disorders in the medical home: an algorithm for developmental surveillance and screening.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Autistic behavior in children with fragile X syndrome: prevalence, stability, and the impact of FMRP.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Video analysis of sensory-motor features in infants with fragile X syndrome at 9-12 months of age.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Pediatricians' reported practices regarding developmental screening: do guidelines work? Do they help?

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Academic skills of boys with fragile X syndrome: profiles and predictors.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Mapping nonverbal IQ in young boys with fragile X syndrome.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Autism spectrum disorder in fragile X syndrome: communication, social interaction, and specific behaviors.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

A prospective longitudinal study of early cognitive development in tuberous sclerosis - a clinic based study.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Developmental screening and detection of developmental delays in infants and toddlers with fragile X syndrome.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Discovering fragile X syndrome: family experiences and perceptions.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Autistic behavior, FMR1 protein, and developmental trajectories in young males with fragile X syndrome.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Early developmental trajectories of males with fragile X syndrome.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2734125

Genetic and environmental influences on the cognitive outcomes of children with fragile X syndrome

2 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19074489

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/JPEPSY/JSN129

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19074489%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19074489%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

PubMed publication ID

19074489

1 reference