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

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Language	Label	Description	Also known as
English	Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

1

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Europe PubMed Central

PubMed publication ID

1 July 2017

author name string

Takao A

2

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

Wilson D

3

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

Cross I

4

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

Momma K

5

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

Wadey R

6

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

Scambler P

7

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

Goodship J

8

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

language of work or name

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publication date

1 October 1993

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Europe PubMed Central

PubMed publication ID

1 July 2017

Journal of Medical Genetics

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Europe PubMed Central

PubMed publication ID

1 July 2017

30

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Europe PubMed Central

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1 July 2017

10

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Europe PubMed Central

PubMed publication ID

1 July 2017

822-824

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Europe PubMed Central

PubMed publication ID

1 July 2017

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

1 reference

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

20 March 2017

DiGeorge syndrome: part of CATCH 22.

1 reference

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

29 September 2017

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

1 reference

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

29 September 2017

A prospective cytogenetic study of 36 cases of DiGeorge syndrome

1 reference

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

29 September 2017

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

1 reference

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

29 September 2017

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

1 reference

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

2 June 2018

Identifiers

10.1136/JMG.30.10.822

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

ResearchGate publication ID

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