(Q72554338)

English

The Nägeli-Franceschetti-Jadassohn syndrome: A hereditary ectodermal defect leading to colloid-amyloid formation in the dermis

scientific article published on 01 January 1993

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Europe PubMed Central

PubMed publication ID

8219417

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219417%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

title

The Nägeli-Franceschetti-Jadassohn syndrome: A hereditary ectodermal defect leading to colloid-amyloid formation in the dermis (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8219417

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219417%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

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E Frenk

1

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Europe PubMed Central

PubMed publication ID

8219417

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219417%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

B Mevorah

series ordinal

2

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Europe PubMed Central

PubMed publication ID

8219417

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219417%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

D Hohl

series ordinal

3

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PubMed publication ID

8219417

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219417%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

publication date

1 January 1993

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Europe PubMed Central

PubMed publication ID

8219417

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219417%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

1 reference

Europe PubMed Central

PubMed publication ID

8219417

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219417%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

volume

187

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Europe PubMed Central

PubMed publication ID

8219417

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219417%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

issue

3

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Europe PubMed Central

PubMed publication ID

8219417

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219417%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

page(s)

169-173

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Europe PubMed Central

PubMed publication ID

8219417

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219417%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

Identifiers

DOI

10.1159/000247236

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8219417

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219417%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

PubMed publication ID

8219417

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8219417

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219417%20AND%20SRC:MED&resulttype=core&format=json

(Q72554338)

The Nägeli-Franceschetti-Jadassohn syndrome: A hereditary ectodermal defect leading to colloid-amyloid formation in the dermis

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