Genetic and molecular diversity in nondeletion Hb H disease (Q36370539)

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English	Genetic and molecular diversity in nondeletion Hb H disease	scientific article

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scholarly article

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Europe PubMed Central

PMC publication ID

348878

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13 August 2017

title

Genetic and molecular diversity in nondeletion Hb H disease (English)

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Europe PubMed Central

PMC publication ID

348878

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13 August 2017

main subject

molecular diversity

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author name string

Higgs DR

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1

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Europe PubMed Central

PMC publication ID

348878

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13 August 2017

Pressley L

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2

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Europe PubMed Central

PMC publication ID

348878

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13 August 2017

Aldridge B

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3

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Europe PubMed Central

PMC publication ID

348878

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13 August 2017

Clegg JB

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4

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Europe PubMed Central

PMC publication ID

348878

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13 August 2017

Weatherall DJ

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5

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Europe PubMed Central

PMC publication ID

348878

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13 August 2017

Cao A

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6

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PMC publication ID

348878

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13 August 2017

Hadjiminas MG

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7

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348878

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Kattamis C

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8

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Europe PubMed Central

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348878

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Metaxatou-Mavromati A

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9

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Europe PubMed Central

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348878

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Rachmilewitz EA

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10

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348878

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Sophocleous T

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11

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Europe PubMed Central

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348878

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13 August 2017

language of work or name

English

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publication date

1 September 1981

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Europe PubMed Central

PMC publication ID

348878

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13 August 2017

published in

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

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Europe PubMed Central

PMC publication ID

348878

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13 August 2017

volume

78

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Europe PubMed Central

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348878

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13 August 2017

issue

9

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Europe PubMed Central

PMC publication ID

348878

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13 August 2017

page(s)

5833-5837

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Europe PubMed Central

PMC publication ID

348878

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13 August 2017

cites work

The 3' untranslated regions of the duplicated human alpha-globin genes are unexpectedly divergent

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=348878

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30 September 2017

Partial deletion of the alpha-globin structural gene in human alpha-thalassaemia

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PubMed Central

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30 September 2017

Characterisation of a new α thalassemia 1 defect due to a partial deletion of the α globin gene complex

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=348878

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30 September 2017

Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=348878

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30 September 2017

Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes

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PubMed Central

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30 September 2017

The duplicated human alpha globin genes lie close together in cellular DNA

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=348878

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30 September 2017

The α-chain-termination mutants and their relation to the α-thalassaemias

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30 September 2017

Hereditary persistence of fetal haemoglobin (HPFH) and delta beta thalassaemia

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PubMed Central

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30 September 2017

beta 0 thalassemia, a nonsense mutation in man

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=348878

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30 September 2017

The chromosomal arrangement of human alpha-like globin genes: sequence homology and alpha-globin gene deletions

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=348878

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28 June 2018

The molecular basis of α-thalassemias: Frequent occurrence of dysfunctional α loci among non-Asians with Hb H disease

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=348878

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28 June 2018

Characterization of beta-globin mRNA in the beta0 thalassemias

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6272319

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12 December 2020

based on heuristic

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Molecular basis of hemoglobin-H disease in the Mediterranean population

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/6272319

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12 December 2020

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A novel α-globin gene arrangement in man

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6272319

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of alpha thalassaemia phenotypes by messenger RNA analysis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6272319

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A New Genetic Basis for Hemoglobin-H Disease

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6272319

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis for the haemoglobin Bart's hydrops fetalis syndrome in Cyprus

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6272319

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a nondeletion defect in alpha-thalassemia

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6272319

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1073/PNAS.78.9.5833

1 reference

stated in

Europe PubMed Central

PMC publication ID

348878

retrieved

13 August 2017

ADS bibcode

1981PNAS...78.5833H

0 references

PMC publication ID

348878

1 reference

stated in

Europe PubMed Central

PMC publication ID

348878

retrieved

13 August 2017

PubMed publication ID

6272319

1 reference

stated in

Europe PubMed Central

PMC publication ID

348878

retrieved

13 August 2017

ResearchGate publication ID

235616958

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