(Q33676947)

28 July 2017

title

Clinical features and reproductive patterns in fragile X female heterozygotes (English)

1 reference

https://api.crossref.org/works/10.1136/JMG.25.6.407

28 July 2017

1 reference

5 January 2023

1

D. Z. Loesch

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3398009

5 January 2023

author name string

D. A. Hay

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3398009

5 January 2023

language of work or name

English

0 references

publication date

1 June 1988

1 reference

full work available at URL

28 July 2017

http://jmg.bmjjournals.com/cgi/content/abstract/25/6/407

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3398009

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/3398009/pdf/?tool=EBI

5 January 2023

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3398009

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/3398009/?tool=EBI

5 January 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3398009

https://europepmc.org/articles/PMC1050510

5 January 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3398009

https://europepmc.org/articles/PMC1050510?pdf=render

5 January 2023

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3398009

https://syndication.highwire.org/content/doi/10.1136/jmg.25.6.407

5 January 2023

1 reference

https://api.crossref.org/works/10.1136/JMG.25.6.407

Journal of Medical Genetics

5 January 2023

published in

1 reference

28 July 2017

volume

25

1 reference

28 July 2017

issue

6

1 reference

28 July 2017

page(s)

407-414

1 reference

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

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050510

Marker (X)-Linked Mental Retardation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050510

The female and the fragile X. A study of 144 obligate female carriers.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050510

Cognitive profiles and the spectrum of clinical manifestations in heterozygous fra (X) females.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050510

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050510

Individual variation and specific cognitive deficits in the fra(X) syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050510

Phenotypic variation in male-transmitted fragile X: genetic inferences.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050510

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050510

CONGENITAL ANOMALIES IN THE NEWBORN INFANT, INCLUDING MINOR VARIATIONS. A STUDY OF 4,412 BABIES BY SURFACE EXAMINATION FOR ANOMALIES AND BUCCAL SMEAR FOR SEX CHROMATIN

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3398009

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Detection of the fragile X chromosome and other fragile sites

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3398009

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.25.6.407

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=3398009

5 January 2023

1 reference

28 July 2017

1 reference