(Q37480082)

20 August 2017

Expression of two X-linked genes in human hair follicles of double heterozygotes (English)

1 reference

20 August 2017

Goldstein JL

1

1 reference

20 August 2017

Marks JF

series ordinal

2

1 reference

20 August 2017

Gartler SM

series ordinal

3

1 reference

20 August 2017

language of work or name

English

0 references

publication date

1 July 1971

1 reference

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

20 August 2017

1 reference

20 August 2017

68

1 reference

20 August 2017

7

1 reference

20 August 2017

1425-1427

1 reference

DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=389209

Mitotic separation of two human X-linked genes in man--mouse somatic cell hybrids

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=389209

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=389209

Hurler's syndrome: a genetic study of clones in cell culture with particular reference to the Lyon hypothesis

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=389209

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=389209

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

26 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/5283930

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/5283930

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/5283930

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.68.7.1425

1 reference

20 August 2017

0 references

1 reference

20 August 2017

PubMed publication ID

5283930

1 reference