(Q70953358)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8582397%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

title

Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8582397%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

author name string

K Takahashi

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8582397%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

S Kido

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8582397%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

K Hoshino

3

1 reference

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15 October 2019

K Ogawa

4

1 reference

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15 October 2019

H Ohashi

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8582397%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

Y Fukushima

6

1 reference

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15 October 2019

publication date

1 November 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8582397%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Pediatrics

15 October 2019

published in

1 reference

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15 October 2019

volume

154

1 reference

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15 October 2019

issue

11

1 reference

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15 October 2019

page(s)

878-881

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf01957496

15 October 2019

exact match

0 references

cites work

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

DiGeorge syndrome: part of CATCH 22.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01957496

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8582397%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

1 reference