(Q53292316)

English

MEGDEL Syndrome: Expanding the Phenotype and New Mutations.

scientific article published on 15 May 2017

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scholarly article

1 reference

stated in

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/MED/28505671

title

MEGDEL Syndrome: Expanding the Phenotype and New Mutations. (English)

1 reference

stated in

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/MED/28505671

author

Sandra Jacinto

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed ID

28505671

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28505671%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 June 2020

Ron A. Wevers

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4

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stated in

Europe PubMed Central

PubMed ID

28505671

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28505671%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 June 2020

author name string

Sílvia Sequeira

series ordinal

1

1 reference

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Europe PubMed Central

PubMed ID

28505671

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28505671%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 June 2020

Márcia Rodrigues

series ordinal

2

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Europe PubMed Central

PubMed ID

28505671

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28505671%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 June 2020

Saskia B Wortmann

series ordinal

5

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stated in

Europe PubMed Central

PubMed ID

28505671

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28505671%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 June 2020

publication date

15 May 2017

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stated in

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/MED/28505671

published in

Neuropediatrics

1 reference

stated in

Europe PubMed Central

PubMed ID

28505671

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28505671%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 June 2020

volume

48

1 reference

stated in

Europe PubMed Central

PubMed ID

28505671

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28505671%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 June 2020

issue

5

1 reference

stated in

Europe PubMed Central

PubMed ID

28505671

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28505671%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 June 2020

page(s)

382-384

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stated in

Europe PubMed Central

PubMed ID

28505671

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28505671%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 June 2020

Identifiers

DOI

10.1055/S-0037-1602833

1 reference

stated in

Europe PubMed Central

PubMed ID

28505671

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28505671%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

1 reference

Europe PubMed Central

PubMed ID

28505671

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28505671%20AND%20SRC:MED&resulttype=core&format=json

(Q53292316)

MEGDEL Syndrome: Expanding the Phenotype and New Mutations.

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