(Q69982540)

English

Severe hemochromatosis: the predominant clinical manifestation of congenital dyserythropoietic anemia type 2

scientific article published on 01 January 1985

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scholarly article

1 reference

stated in

Europe PubMed Central

PubMed ID

3938164

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3938164%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 October 2019

title

Severe hemochromatosis: the predominant clinical manifestation of congenital dyserythropoietic anemia type 2 (English)

1 reference

stated in

Europe PubMed Central

PubMed ID

3938164

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3938164%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 October 2019

main subject

congenital dyserythropoietic anemia

1 reference

Z Halpern

1

1 reference

stated in

Europe PubMed Central

PubMed ID

3938164

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3938164%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 October 2019

R Rahmani

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed ID

3938164

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3938164%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 October 2019

Y Levo

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed ID

3938164

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3938164%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 October 2019

publication date

1 January 1985

1 reference

stated in

Europe PubMed Central

PubMed ID

3938164

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3938164%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

1 reference

Europe PubMed Central

PubMed ID

3938164

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3938164%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 October 2019

volume

74

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stated in

Europe PubMed Central

PubMed ID

3938164

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3938164%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 October 2019

issue

3

1 reference

stated in

Europe PubMed Central

PubMed ID

3938164

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3938164%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 October 2019

page(s)

178-180

1 reference

stated in

Europe PubMed Central

PubMed ID

3938164

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3938164%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 October 2019

Identifiers

DOI

10.1159/000206205

1 reference

stated in

Europe PubMed Central

PubMed ID

3938164

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3938164%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

1 reference

Europe PubMed Central

PubMed ID

3938164

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3938164%20AND%20SRC:MED&resulttype=core&format=json

(Q69982540)

Severe hemochromatosis: the predominant clinical manifestation of congenital dyserythropoietic anemia type 2

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