Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11 (Q28255966)

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English	Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11	scientific article

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scholarly article

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

title

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

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

author

John Burn

series ordinal

1

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stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

Peter J Scambler

series ordinal

7

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

Judith A Goodship

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8

object named as

J Goodship

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

author name string

A Takao

series ordinal

2

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

D Wilson

series ordinal

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

I Cross

series ordinal

4

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

K Momma

series ordinal

5

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

R Wadey

series ordinal

6

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

language of work or name

English

0 references

publication date

1 October 1993

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

published in

Journal of Medical Genetics

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

volume

30

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

issue

10

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

page(s)

822-824

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

cites work

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

20 March 2017

DiGeorge syndrome: part of CATCH 22.

1 reference

stated in

PubMed Central

reference URL

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

retrieved

29 September 2017

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

29 September 2017

A prospective cytogenetic study of 36 cases of DiGeorge syndrome

1 reference

stated in

PubMed Central

reference URL

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

retrieved

29 September 2017

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

29 September 2017

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

2 June 2018

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

1 reference

stated in

PubMed

reference URL

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

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions within chromosome 22q11 in familial congenital heart disease

1 reference

stated in

PubMed

reference URL

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

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1136/JMG.30.10.822

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

OpenCitations bibliographic resource ID

5106435

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

5106435

PMC publication ID

1016562

2 references

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

5106435

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

PubMed publication ID

8230157

1 reference

stated in

Europe PubMed Central

PMC publication ID

1016562

reference URL

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

retrieved

27 October 2019

ResearchGate publication ID

14969445

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