Hair root versus red cell individual phenotype in Sardinian heterozygotes for G6PD deficiency (Mediterranean type). (Q35201620)

7 August 2017

title

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

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7 August 2017

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Romeo G

1

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7 August 2017

Rinaldi A

series ordinal

2

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7 August 2017

Urbano F

series ordinal

3

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7 August 2017

Filippi G

series ordinal

4

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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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American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

28

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7 August 2017

issue

5

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7 August 2017

page(s)

506-513

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Cytological and biochemical correlation of late X-chromosome replication and gene inactivation in the mule

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685099

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685099

Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685099

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685099

X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685099

Primordial cell pool size and lineage relationships of five human cell types

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685099

Glycogen-storage disease associated with phosphorylase kinase deficiency: evidence for X inactivation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685099

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685099

Glucose-6-phosphate dehydrogenase mosaicism: ito;ozatopm om tje study of hair follicle variegation

13 July 2018

1 reference

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

26 September 2018

1 reference

12 December 2020

Sex differences in activity of glucose 6-phosphate dehydrogenase from cultured human fetal lung cells despite X-inactivation

1 reference

12 December 2020

Human phosphoglycerate kinase and inactivation of the X chromosome

1 reference

12 December 2020

Mosaicism for sulfoiduronate sulfatase deficiency in carriers of Hunter's syndrome

1 reference

12 December 2020

Lesch-Nyhan Syndrome: Rapid Detection of Heterozygotes by Use of Hair Follicles

1 reference

12 December 2020

Genetic Inactivation of the α-Galactosidase Locus in Carriers of Fabry's Disease

1 reference

12 December 2020

Identifiers

PMC publication ID

1685099

1 reference

7 August 2017

1 reference