Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia (Q35201667)

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English	Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia	scientific article

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PubMed publication ID

984045

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7 August 2017

title

Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia (English)

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Europe PubMed Central

PubMed publication ID

984045

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7 August 2017

main subject

bias

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author name string

Rinaldi A

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1

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Europe PubMed Central

PubMed publication ID

984045

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7 August 2017

Filippi G

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2

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Europe PubMed Central

PubMed publication ID

984045

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7 August 2017

Siniscalco M

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3

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PubMed publication ID

984045

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7 August 2017

language of work or name

English

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publication date

1 September 1976

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Europe PubMed Central

PubMed publication ID

984045

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7 August 2017

published in

American Journal of Human Genetics

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Europe PubMed Central

PubMed publication ID

984045

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7 August 2017

volume

28

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Europe PubMed Central

PubMed publication ID

984045

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7 August 2017

issue

5

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Europe PubMed Central

PubMed publication ID

984045

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7 August 2017

page(s)

496-505

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Europe PubMed Central

PubMed publication ID

984045

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7 August 2017

cites work

Studies of Glucose-6-Phosphate Dehydrogenase Activity of Individual Erythrocytes: The Methemoglobin-Elution Test for Identification of Females Heterozygous for G6PD Deficiency

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=1685117

retrieved

13 July 2018

DISTRIBUTION OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE ELECTROPHORETIC VARIANTS IN DIFFERENT TISSUES OF HETEROZYGOTES

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685117

retrieved

13 July 2018

Characterization of glucose-6-phosphate dehydrogenase variants. I. Occurrence of a G6PD Seattle-like variant in Sardinia and its interaction with the G6PD Mediterranean variant

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=1685117

retrieved

13 July 2018

Failure to detect linkage between Xg and other X-borne loci in Sardinians

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=1685117

retrieved

13 July 2018

Population genetics of haemoglobin variants, thalassaemia and glucose-6-phosphate dehydrogenase deficiency, with particular reference to the malaria hypothesis

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=1685117

retrieved

13 July 2018

Hemizygous expression of glucose-6-phosphate dehydrogenase in erythrocytes of heterozygotes for the Lesch-Nyhan syndrome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685117

retrieved

13 July 2018

Developmental implications of multiple tissue studies in glucose-6-phosphate dehydrogenase-deficient heterozygotes

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=1685117

retrieved

13 July 2018

Studies of skin fibroblasts from 10 families with HGPRT deficiency, with reference in X-chromosomal inactivation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685117

retrieved

13 July 2018

Glucose-6-Phosphate Dehydrogenase Deficient Red Cells: Resistance to Infection by Malarial Parasites

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685117

retrieved

13 July 2018

Mosaicism of peripheral blood lymphocyte populations in females heterozygous for the Lesch-Nyhan mutation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685117

retrieved

13 July 2018

Lesch-Nyhan syndrome: absence of the mutant enzyme in erythrocytes of a heterozygote for both normal and mutant hypoxanthine-guanine phosphoribosyl transferase.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685117

retrieved

13 July 2018

Hair root versus red cell individual phenotype in Sardinian heterozygotes for G6PD deficiency (Mediterranean type).

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685117

retrieved

13 July 2018

Glucose-6 phosphate dehydrogenase mosaicism: utilization as a tracer in the study of the development of hair root cells

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/984045

retrieved

12 December 2020

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GENETIC TESTS WITH A SEX-LINKED MARKER: GLUCOSE-6-PHOSPHATE DEHYDROGENASE

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/984045

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12 December 2020

based on heuristic

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SELECTION IN MAMMALIAN MOSAIC CELL POPULATIONS

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/984045

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12 December 2020

based on heuristic

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SURVIVAL OF 51 CR-LABELLED RED CELLS IN SUBJECTS WITH THALASSAEMIA-TRAIT OR G6PD DEFICIENCY OR BOTH ABNORMALITIES

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/984045

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12 December 2020

based on heuristic

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The Haematological Effects of Glucose-6-Phosphate Dehydrogenase Deficiency and Thalassaemia Trait: Interaction between the Two Genes at the Phenotype Level

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/984045

retrieved

12 December 2020

based on heuristic

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Identifiers

PMC publication ID

1685117

1 reference

stated in

Europe PubMed Central

PubMed publication ID

984045

retrieved

7 August 2017

PubMed publication ID

984045

1 reference

stated in

Europe PubMed Central

PubMed publication ID

984045

retrieved

7 August 2017

 

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