(Q78074946)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11998920%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

title

Familial 22q11.2 deletion: an infant with interrupted aortic arch and DiGeorge syndrome delivered from by a mother with tetralogy of Fallot (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11998920%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

1 reference

1 reference

interrupted aortic arch

1 reference

Tadahiko Ito

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11998920%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

Tadashi Okubo

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11998920%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

Hiroshi Sato

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11998920%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

publication date

1 March 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11998920%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Pediatrics

10 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11998920%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

volume

161

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11998920%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11998920%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

page(s)

173-174

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11998920%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00431-001-0890-8

10 December 2019

exact match

0 references

cites work

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

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00431-001-0890-8

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00431-001-0890-8

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00431-001-0890-8