(Q55388896)

English

Haemoglobin H disease with persistent haemoglobin "Bart's" in an Oriental Jewess and her daughter: a dual alpha-chain deficiency of human haemoglobin.

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

Haemoglobin H disease with persistent haemoglobin "Bart's" in an Oriental Jewess and her daughter: a dual alpha-chain deficiency of human haemoglobin. (English)

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

author name string

RAMOT B

1

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

SHEBA C

2

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

FISHER S

3

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

AGER JA

4

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

LEHMANN H

5

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

language of work or name

0 references

publication date

1 December 1959

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

2

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

5161

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

1228-1230

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1991468

12 August 2018

Observations on some fast haemoglobins: K, J, N, and Bart's.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1991468

12 August 2018

Thalassemia in Jews from Kurdistan

1 reference

https://pubmed.ncbi.nlm.nih.gov/14436101

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identity of the α-Chains of Adult and Fœtal Human Hæmoglobins

1 reference

https://pubmed.ncbi.nlm.nih.gov/14436101

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New hemoglobin possessing a higher electrophoretic mobility than normal adult hemoglobin

1 reference

https://pubmed.ncbi.nlm.nih.gov/14436101

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The amino-acid composition of human adult and foetal carbonmonoxyhaemoglobin extimated by ion exchange chromatography

1 reference

https://pubmed.ncbi.nlm.nih.gov/14436101

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selective occurrence of glutathione instability in red blood corpuscles of the various Jewish tribes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14436101

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and Hæmatological Significance of Hæmoglobin H

1 reference

https://pubmed.ncbi.nlm.nih.gov/14436101

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal Human Hæmoglobins: Hæmoglobin ‘Bart's’: a Fœtal Hæmoglobin without α-Chains

1 reference

https://pubmed.ncbi.nlm.nih.gov/14436101

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Persistence of haemoglobin "Bart's" beyond infancy in a child with thalassaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/14436101

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Description of a new variety of congenital hemolytic anemia; hematologic study, electrophoretic and genetic]

1 reference

https://pubmed.ncbi.nlm.nih.gov/14436101

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/BMJ.2.5161.1228

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

5 July 2018

http://europepmc.org/abstract/PMC/1991468

ResearchGate publication ID

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