(Q33712206)

28 July 2017

title

Studies on the Hemoglobin of Cooley's Anemia and Cooley's Trait (English)

1 reference

28 July 2017

Rich A

1

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 March 1952

1 reference

Proceedings of the National Academy of Sciences of the United States of America

28 July 2017

published in

1 reference

28 July 2017

volume

38

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28 July 2017

issue

3

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28 July 2017

page(s)

187-196

1 reference

Further Studies on the Genetics of Thalassemia.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1063532

The steady state, a test for electrophoretic homogeneity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1063532

Electrophoretic studies on human serum albumin

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1063532

The haemoglobin of the human foetus and infant. Electrophoretic and spectroscopic differentiation of adult and foetal types

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1063532

Presence of Foetal Haemoglobin in Cooley's anaemia.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1063532

Studies on abnormal hemoglobins. II. Their identification by means of the method of fractional denaturation.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1063532

Erythrocyte survival studies in childhood. II. Studies in Mediterranean anemia

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16589079

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The inheritance of the sickling phenomenon, with particular reference to sickle cell disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16589079

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.38.3.187

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28 July 2017

0 references

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28 July 2017

1 reference