(Q35197904)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2309697%20AND%20SRC:MED&resulttype=core&format=json

26 September 2019

title

Population genetic consequences of the fragile-X syndrome, based on the X-inactivation imprinting model (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2309697%20AND%20SRC:MED&resulttype=core&format=json

26 September 2019

0 references

1 reference

Sved JA

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2309697%20AND%20SRC:MED&resulttype=core&format=json

26 September 2019

Laird CD

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2309697%20AND%20SRC:MED&resulttype=core&format=json

26 September 2019

language of work or name

English

0 references

publication date

1 March 1990

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2309697%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

26 September 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2309697%20AND%20SRC:MED&resulttype=core&format=json

26 September 2019

volume

46

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2309697%20AND%20SRC:MED&resulttype=core&format=json

26 September 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2309697%20AND%20SRC:MED&resulttype=core&format=json

26 September 2019

page(s)

443-451

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2309697%20AND%20SRC:MED&resulttype=core&format=json

Mutation and selection in the marker (X) syndrome. A hypothesis

26 September 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683633

A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683633

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683633

Proposed mechanism of inheritance and expression of the human fragile-X syndrome of mental retardation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683633

Population genetics implications of the premutation hypothesis for the generation of the fragile X mental retardation gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683633

Fragile X families in a northern Swedish county--a genealogical study demonstrating apparent paternal transmission from the 18th century

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683633

Genetics and expression of the fragile X syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683633

Selection and mutation at an X-linked locus

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683633

The marker (X) syndrome: a cytogenetic and genetic analysis.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683633

26 September 2018

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2309697%20AND%20SRC:MED&resulttype=core&format=json

26 September 2019

PubMed publication ID

2309697

1 reference