(Q33668979)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7328617%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

title

The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7328617%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7328617

7 May 2024

author name string

R. Proops

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7328617

7 May 2024

T. Webb

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7328617

7 May 2024

language of work or name

English

0 references

publication date

1 October 1981

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7328617%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

15 October 2019

https://jmg.bmj.com/content/18/5/366.full.pdf

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7328617

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/7328617/pdf/?tool=EBI

7 May 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7328617

http://jmg.bmjjournals.com/cgi/content/abstract/18/5/366

7 May 2024

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%3A7328617

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/7328617/?tool=EBI

7 May 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7328617

https://europepmc.org/articles/PMC1048759

7 May 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7328617

https://europepmc.org/articles/PMC1048759?pdf=render

7 May 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7328617

https://syndication.highwire.org/content/doi/10.1136/jmg.18.5.366

7 May 2024

1 reference

https://api.crossref.org/works/10.1136/JMG.18.5.366

Journal of Medical Genetics

7 May 2024

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7328617%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

volume

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7328617%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7328617%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

page(s)

366-373

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7328617%20AND%20SRC:MED&resulttype=core&format=json

Familial sex-linked mental retardation

15 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048759

Testicular size: assessment and clinical importance

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048759

21 June 2018

A marker X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048759

X-linked Mental Retardation Without Physical Abnormality: Renpenning's 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=1048759

Testicular volume during adolescence. Cross-sectional and longitudinal studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048759

X-linked mental retardation and verbal disability

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048759

X-linked mental retardation associated with macro-orchidism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048759

Familial X-linked mental retardation with an X chromosome abnormality

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048759

More on marker X chromosomes, mental retardation and macro-orchidism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048759

Marker X chromosomes, mental retardation and macro-orchidism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048759

X-Linked mental retardation with macro-orchidism and the fragile site at Xq27 or 28

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048759

Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048759

Familial X-linked mental retardation, verbal disability, and marker X chromosomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048759

Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048759

Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048759

Developmental dyspraxia in a family with X-linked mental retardation (Renpenning 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=1048759

Cytogenetic observations in vitamin B12 and folate deficiency

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7328617

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A rapid banding technique for human chromosomes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7328617

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

series ordinal

3

1 reference

https://api.crossref.org/works/10.1136/JMG.18.5.366

7 May 2024

Identifiers

DOI

10.1136/JMG.18.5.366

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7328617%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7328617%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

1 reference