(Q72553891)

English

Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis

scientific article published on 01 November 1993

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scholarly article

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Europe PubMed Central

PubMed ID

8219186

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219186%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

title

Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis (English)

1 reference

stated in

Europe PubMed Central

PubMed ID

8219186

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219186%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

main subject

hereditary spherocytosis

1 reference

Savvides P

1

1 reference

stated in

Europe PubMed Central

PubMed ID

8219186

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219186%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

Shalev O

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed ID

8219186

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219186%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

John KM

series ordinal

3

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stated in

Europe PubMed Central

PubMed ID

8219186

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219186%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

Lux SE

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed ID

8219186

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219186%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

language of work or name

English

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publication date

1 November 1993

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stated in

Europe PubMed Central

PubMed ID

8219186

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219186%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

1 reference

Europe PubMed Central

PubMed ID

8219186

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219186%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

volume

82

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Europe PubMed Central

PubMed ID

8219186

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219186%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

issue

10

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Europe PubMed Central

PubMed ID

8219186

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219186%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

page(s)

2953-2960

1 reference

stated in

Europe PubMed Central

PubMed ID

8219186

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219186%20AND%20SRC:MED&resulttype=core&format=json

retrieved

27 October 2019

Identifiers

PubMed ID

8219186

1 reference

stated in

Europe PubMed Central

PubMed ID

8219186

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8219186%20AND%20SRC:MED&resulttype=core&format=json

(Q72553891)

Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis

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