(Q79497262)

English

Familial hypohaptoglobinemia. A genetically determined trait segragating from glucose-6-phosphate dehydrogenase deficiency

scientific article published on 01 February 1963

In more languages

edit

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

13949483

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13949483%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 December 2019

title

Familial hypohaptoglobinemia. A genetically determined trait segragating from glucose-6-phosphate dehydrogenase deficiency (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

13949483

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13949483%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 December 2019

main subject

glucose-6-phosphate dehydrogenase deficiency

0 references

author name string

GOTTLIEB A

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

13949483

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13949483%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 December 2019

WISCH N

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

13949483

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13949483%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 December 2019

ROSS J

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

13949483

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13949483%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 December 2019

publication date

1 February 1963

1 reference

stated in

Europe PubMed Central

PubMed publication ID

13949483

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13949483%20AND%20SRC:MED&resulttype=core&format=json

23 December 2019

1 reference

Europe PubMed Central

PubMed publication ID

13949483

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13949483%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 December 2019

volume

21

1 reference

stated in

Europe PubMed Central

PubMed publication ID

13949483

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13949483%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 December 2019

page(s)

129-140

1 reference

stated in

Europe PubMed Central

PubMed publication ID

13949483

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13949483%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 December 2019

Identifiers

PubMed publication ID

13949483

1 reference

stated in

Europe PubMed Central

PubMed publication ID

13949483

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13949483%20AND%20SRC:MED&resulttype=core&format=json

(Q79497262)

Familial hypohaptoglobinemia. A genetically determined trait segragating from glucose-6-phosphate dehydrogenase deficiency

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)