(Q28255966)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

title

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11 (English)

1 reference

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27 October 2019

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

Peter J Scambler

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

8

J Goodship

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

author name string

A Takao

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

D Wilson

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

I Cross

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

K Momma

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

R Wadey

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

language of work or name

English

0 references

publication date

1 October 1993

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

Journal of Medical Genetics

27 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

volume

30

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

issue

10

1 reference

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27 October 2019

page(s)

822-824

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome

27 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=1016562

DiGeorge syndrome: part of CATCH 22.

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016562

Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016562

A prospective cytogenetic study of 36 cases of DiGeorge syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016562

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016562

Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016562

Systemic treatment of early breast cancer by hormonal, cytotoxic, or immune therapy. 133 randomised trials involving 31,000 recurrences and 24,000 deaths among 75,000 women. Early Breast Cancer Trialists' Collaborative Group

2 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8230157

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Deletions within chromosome 22q11 in familial congenital heart disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8230157

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.30.10.822

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

OpenCitations bibliographic resource ID

27 October 2019

5106435

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

5106435

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230157%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

PubMed publication ID

8230157

1 reference