(Q74449041)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12112447%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

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title

Neurobiology of Fragile X syndrome: from molecular genetics to neurobehavioral phenotype (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12112447%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

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Walter E Kaufmann

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12112447%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

publication date

1 May 2002

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12112447%20AND%20SRC:MED&resulttype=core&format=json

Microscopy Research and Technique

10 November 2019

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12112447%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

volume

57

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12112447%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

issue

3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12112447%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

page(s)

131-134

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12112447%20AND%20SRC:MED&resulttype=core&format=json

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

10 November 2019

cites work

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https://api.crossref.org/works/10.1002%2FJEMT.10065

Analysis of neocortex in three males with the fragile X syndrome

21 January 2018

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https://api.crossref.org/works/10.1002%2FJEMT.10065

Dendritic spine structural anomalies in fragile-X mental retardation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10065

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10065

Dendritic anomalies in disorders associated with mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10065

Molecular and cellular genetics of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10065

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/10.1002%2FJEMT.10065

Premature ovarian failure in the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10065

Transcription of the FMR1 gene in individuals with fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10065

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%2FJEMT.10065

21 January 2018

Identifiers

DOI

10.1002/JEMT.10065

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12112447%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference