(Q34986463)

5 August 2017

title

13q- syndrome. Family study (English)

1 reference

5 August 2017

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%3A606176

4 August 2023

A. Carmichael

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A606176

4 August 2023

D. P. Addy

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A606176

4 August 2023

W. R. Shortland-Webb

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A606176

4 August 2023

A. H. Cameron

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A606176

4 August 2023

I. C. Davies

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A606176

4 August 2023

language of work or name

English

0 references

publication date

1 December 1977

1 reference

full work available at URL

5 August 2017

https://europepmc.org/articles/PMC1545016

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A606176

https://europepmc.org/articles/PMC1545016?pdf=render

4 August 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%3A606176

https://syndication.highwire.org/content/doi/10.1136/adc.52.12.972

4 August 2023

1 reference

Crossref

DOI

https://api.crossref.org/works/10.1136/ADC.52.12.972

Archives of Disease in Childhood

4 August 2023

published in

1 reference

5 August 2017

1 reference

5 August 2017

1 reference

5 August 2017

page(s)

972-974

1 reference

The 13q-deletion syndrome

5 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545016

The 13q- deletion syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545016

D13 ring chromosome syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545016

New Chromosomal Syndromes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545016

[Partial 13 trisomy by maternal 46, XX, t (3; 13) (p 26; q 21) translocation]

8 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/606176

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Partial monosomy 13 as the result of a balanced translocation 3/13 pat

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/606176

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Pulmonary hemorrhage and death complicating anaphylactoid purpura

1 reference

https://api.crossref.org/works/10.1136/ADC.52.12.972

Henoch-Schoenlein Syndrome

4 August 2023

1 reference

https://api.crossref.org/works/10.1136/ADC.52.12.972

Human chromosomes and their anomalies

4 August 2023

1 reference

https://api.crossref.org/works/10.1136/ADC.52.12.972

4 August 2023

Identifiers

DOI

1 reference

5 August 2017

1 reference

5 August 2017

1 reference