(Q35570555)

8 August 2017

title

Half chromatid mutations: transmission in humans? (English)

1 reference

8 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1124765

24 August 2022

author name string

S. M. Gartler

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1124765

24 August 2022

U. Francke

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1124765

24 August 2022

language of work or name

English

0 references

publication date

1 March 1975

1 reference

full work available at URL

8 August 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1124765/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1124765

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1124765/pdf/?tool=EBI

24 August 2022

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1124765

https://europepmc.org/articles/PMC1762757

24 August 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1124765

https://europepmc.org/articles/PMC1762757?pdf=render

24 August 2022

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1124765

American Journal of Human Genetics

24 August 2022

published in

1 reference

8 August 2017

volume

27

1 reference

8 August 2017

issue

2

1 reference

8 August 2017

page(s)

218-223

1 reference

8 August 2017

cites work

Mutation in eukaryotes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762757

Development of a nonselective technique for studying 2, 6, diaminopurine resistance in an established murine cell line

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762757

The Detection of Increased Mutation Rates in Human Populations

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762757

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762757

Mutation and cancer: statistical study of retinoblastoma

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762757

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762757

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762757

Mortality in the children of atomic bomb survivors and controls

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762757

Family studies of a Lesch-Nyhan patient from an isolated Canadian community

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762757

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

12 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1124765

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Detection of heterozygous carriers of the Lesch-Nyhan syndrome by electrophoresis of hair root lysates

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1124765

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Detection of heterozygote in Lesch-Nyhan disease by hair-root analysis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1124765

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1762757

1 reference

8 August 2017

1 reference