(Q34063057)

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

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scholarly article

1 reference

Europe PubMed Central

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

30 July 2017

author name string

Webber SA

1

1 reference

Europe PubMed Central

30 July 2017

Hatchwell E

2

1 reference

Europe PubMed Central

30 July 2017

Barber JC

3

1 reference

Europe PubMed Central

30 July 2017

Daubeney PE

4

1 reference

Europe PubMed Central

30 July 2017

Crolla JA

5

1 reference

Europe PubMed Central

30 July 2017

Salmon AP

6

1 reference

Europe PubMed Central

30 July 2017

Keeton BR

7

1 reference

Europe PubMed Central

30 July 2017

Temple IK

8

1 reference

Europe PubMed Central

30 July 2017

Dennis NR

9

1 reference

Europe PubMed Central

30 July 2017

language of work or name

0 references

publication date

1 July 1996

1 reference

Europe PubMed Central

30 July 2017

The Journal of Pediatrics

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Europe PubMed Central

30 July 2017

129

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30 July 2017

1

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Europe PubMed Central

30 July 2017

26-32

1 reference

Europe PubMed Central

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

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Identifiers

10.1016/S0022-3476(96)70186-5

1 reference

Europe PubMed Central

30 July 2017

1 reference

Europe PubMed Central

30 July 2017

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