(Q33586247)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4548442%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

title

Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4548442%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

1 reference

1 reference

https://api.crossref.org/works/10.1136/JMG.11.4.317

2 February 2023

author name string

R. Skinner

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4548442

2 February 2023

C. Smith

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4548442

2 February 2023

A. E. Emery

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4548442

2 February 2023

language of work or name

English

0 references

publication date

1 December 1974

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4548442%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

29 September 2019

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/4548442/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4548442

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/4548442/pdf/?tool=EBI

2 February 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%3A4548442

https://europepmc.org/articles/PMC1013197

2 February 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4548442

https://europepmc.org/articles/PMC1013197?pdf=render

2 February 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%3A4548442

https://syndication.highwire.org/content/doi/10.1136/jmg.11.4.317

2 February 2023

1 reference

https://api.crossref.org/works/10.1136/JMG.11.4.317

Journal of Medical Genetics

2 February 2023

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4548442%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

volume

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4548442%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4548442%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

page(s)

317-320

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4548442%20AND%20SRC:MED&resulttype=core&format=json

Evidence for the absence of detectable linkage between the genes for Duchenne muscular dystrophy and the Xg blood group

29 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=1013197

New results of genetics of muscular dystrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013197

Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013197

X-linked scapuloperoneal 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=1013197

An improved procedure for serum creatine phosphokinase determination

21 June 2018

1 reference

12 December 2020

A benign X-chromosomal hereditary muscular dystrophy. I. Examinations of symptom-carriers

1 reference

12 December 2020

The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups

1 reference

12 December 2020

Two families of benign sex-linked recessive muscular dystrophy

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.11.4.317

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4548442%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4548442%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

1 reference