(Q58426333)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3411398%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

title

Confirmation of autosomal dominant transmission of the DiGeorge malformation complex (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3411398%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

4

1 reference

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24 September 2019

Connie H. Miller

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3411398%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

author name string

L D Keppen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3411398%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

J W Fasules

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3411398%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

A W Burks

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3411398%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

J R Sawyer

5

1 reference

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24 September 2019

language of work or name

English

0 references

publication date

1 September 1988

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3411398%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Pediatrics

24 September 2019

published in

1 reference

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24 September 2019

volume

113

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3411398%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

page(s)

506-508

1 reference

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24 September 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3411398%20AND%20SRC:MED&resulttype=core&format=json

The spectrum of the DiGeorge syndrome

24 September 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980640-1

A deletion in chromosome 22 can cause DiGeorge syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980640-1

The association of the DiGeorge anomalad with partial monosomy of chromosome 22.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980640-1

Familial DiGeorge syndrome and associated partial monosomy of chromosome 22

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980640-1

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980640-1

Familial third-fourth pharyngeal pouch syndrome with apparent autosomal dominant transmission

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980640-1

Familial thymic aplasia. Attempted reconstitution with fetal thymus in a Millipore diffusion chamber

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980640-1

10.1016/S0022-3476(88)80640-1

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3411398%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

1 reference