(Q73840774)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339379%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

title

Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339379%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference

Momma K

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339379%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Takao A

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339379%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Matsuoka R

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339379%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Imai Y

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339379%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Muto A

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339379%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Osawa M

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339379%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Takayama M

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339379%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

publication date

1 January 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339379%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339379%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

volume

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339379%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339379%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

page(s)

56-60

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339379%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1097/00125817-200101000-00012

7 November 2019

exact match

0 references

cites work

Frequency of 22q11 deletions in patients with conotruncal defects

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012

Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defect.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012

Monosomy 22q11 in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012

Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012

Tetralogy of Fallot associated with chromosome 22q11 deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012

Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012

Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012

Deletion 22q11: a newly recognized cause of behavioral and psychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012

Phenotype of adults with the 22q11 deletion syndrome: A review

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012

Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired".

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012

Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012

Tricuspid atresia in adolescents and adults: current state and late complications

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012

Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00012