(Q77886992)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10370516%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

title

[ Head and truncal abnormalities and secondary clinical aspects of 22q11 microdeletion. A series of 111 patients] (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10370516%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

author name string

G M Brevière

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10370516%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

M F Croquette

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10370516%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

B Delobel

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10370516%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

P Pellerin

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10370516%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

C Rey

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10370516%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

publication date

1 January 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10370516%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

published in

Archives de Pediatrie

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10370516%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

volume

6 Suppl 2

1 reference

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8 December 2019

page(s)

305s-307s

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10370516%20AND%20SRC:MED&resulttype=core&format=json

DiGeorge syndrome: part of CATCH 22.

8 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0929-693X%2899%2980448-5

7 January 2021

Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS0929-693X%2899%2980448-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0929-693X%2899%2980448-5

7 January 2021

The otolaryngologist and the patient with velocardiofacial syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0929-693X%2899%2980448-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0929-693X%2899%2980448-5

7 January 2021

[Microdeletion of the chromosome 22q11 in children: apropos of a series of 49 patients]

1 reference

https://api.crossref.org/works/10.1016%2FS0929-693X%2899%2980448-5

7 January 2021

10.1016/S0929-693X(99)80448-5

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10370516%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

1 reference