(Q71654999)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6822926%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

title

Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6822926%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

1 reference

C S Kitchens

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6822926%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

J A Alexander

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6822926%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

language of work or name

English

0 references

publication date

1 February 1983

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6822926%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Pediatrics

20 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6822926%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

volume

102

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6822926%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6822926%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

page(s)

224-227

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6822926%20AND%20SRC:MED&resulttype=core&format=json

Hypertelorism With Turner Phenotype

20 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980525-3

Noonan syndrome in an adult family presenting with chronic lymphedema

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980525-3

The measurement of factor XI (Plasma thromboplastin antecedent). Diagnosis and therapy of the congenital deficiency state.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980525-3

The Noonan syndrome: a family study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980525-3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980525-3

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-3476(83)80525-3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6822926%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

1 reference