Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study (Q34063057)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

author name string

Webber SA

1

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Hatchwell E

2

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Barber JC

3

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Daubeney PE

4

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Crolla JA

5

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Salmon AP

6

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Keeton BR

7

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Temple IK

8

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Dennis NR

9

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

language of work or name

0 references

publication date

1 July 1996

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

The Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

129

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

26-32

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Deletions within chromosome 22q11 in familial congenital heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Cardiac malformations in the velocardiofacial syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Role of neural crest in congenital heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Velo-cardio-facial syndrome: a review of 120 patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

DiGeorge syndrome: part of CATCH 22.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Fluorodeoxyuridine synchronization of bone marrow cultures

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134).

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Toward a molecular understanding of congenital heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Velocardiofacial syndrome in a mother and daughter: variability of the clinical phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

A familial MCA/MR syndrome due to translocation t(10;16) (q26;p13.1): report of six cases

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

22q11 deletions in isolated and syndromic patients with tetralogy of Fallot

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

The DiGeorge anomaly as a developmental field defect

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970186-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0022-3476(96)70186-5

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34063057&oldid=1577998671"