(Q34635011)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

title

The 13q- deletion syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

main subject

human chromosomes 13-15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142

15 December 2023

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142

15 December 2023

1 reference

https://api.crossref.org/works/10.1136/JMG.8.3.351

15 December 2023

author name string

E. Grace

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142

15 December 2023

J. Drennan

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142

15 December 2023

D. Colver

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142

15 December 2023

R. R. Gordon

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142

15 December 2023

language of work or name

English

0 references

publication date

1 September 1971

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

12 October 2019

https://jmg.bmj.com/content/jmedgenet/8/3/351.full.pdf

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%3A5097142

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5097142/pdf/?tool=EBI

15 December 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%3A5097142

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5097142/?tool=EBI

15 December 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142

https://europepmc.org/articles/PMC1469176

15 December 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142

https://europepmc.org/articles/PMC1469176?pdf=render

15 December 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%3A5097142

https://syndication.highwire.org/content/doi/10.1136/jmg.8.3.351

15 December 2023

1 reference

https://api.crossref.org/works/10.1136/JMG.8.3.351

Journal of Medical Genetics

15 December 2023

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

page(s)

351-357

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json

The Production of Homozygous Deficient Tissues with Mutant Characteristics by Means of the Aberrant Mitotic Behavior of Ring-Shaped Chromosomes

12 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=1469176

CHROMOSOME DELETION IN A CASE OF RETINOBLASTOMA.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469176

Absent thumbs with a ring D2 chromosome: a new deletion syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469176

A human ring D chromosome associated with multiple congenital abnormalities

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469176

A ring D chromosome and anomalous inheritance of haptoglobin type

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469176

The 13q-deletion syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469176

Chromosome abnormalities in two cases with bilateral radial element defects

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469176

Ring chromosomes in two infants with congenital malformations

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469176

Retinoblastoma and deletion D (14) syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469176

Multiple congenital anomalies associated with a ring-D chromosome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469176

The Dr phenotype: a study of threee cases with a ring D chromosome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469176

Ring D1 chromosome and multiple malformations

7 July 2018

1 reference

12 December 2020

Ring D chromosome: a second case associated with anomalous haptoglobin inheritance

1 reference

12 December 2020

The identification of the chromosomes of the D group (13-15) Denver: an autoradiographic and measurement study

1 reference

12 December 2020

A case of D ring chromosome

1 reference

12 December 2020

Multiple congenital abnormalities associated with ring chromosome

1 reference

12 December 2020

Partial deletion of the long arm of a group D (13-15) chromosome :Dq-

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.8.3.351

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

1 reference