(Q35203122)

7 August 2017

title

Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics (English)

1 reference

7 August 2017

1 reference

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A453198

3 July 2022

author name string

G. R. Sutherland

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A453198

3 July 2022

language of work or name

English

0 references

publication date

1 March 1979

1 reference

full work available at URL

7 August 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/453198/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A453198

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/453198/pdf/?tool=EBI

3 July 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A453198

https://europepmc.org/articles/PMC1685761

3 July 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A453198

https://europepmc.org/articles/PMC1685761?pdf=render

3 July 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A453198

American Journal of Human Genetics

3 July 2022

published in

1 reference

7 August 2017

volume

31

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7 August 2017

issue

2

1 reference

7 August 2017

page(s)

136-148

1 reference

7 August 2017

cites work

A marker X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Non-condensation of one segment of a chromosome No. 2 in a male with an otherwise normal karyotype (and severe hypospadias)

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Transformation of foetal human keukocytes in vitro by filtrates of a human leukaemic cell line containing herpes-like virus

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Inherited constriction fragility of chromosome 2.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Correlation between euploid structural chromosome rearrangements and mental subnormality in humans

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Specific instability of the paracentric region of chromosome number 9 in a normal woman and her mongoloid son.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Preferential breakage of sensitive regions of human chromosomes.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Spontaneous fragility of an abnormally wide secondary constriction region in a human chromosome no. 9.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Chromosomal abnormalities and congenital heart disease.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

A homozygous chromosomal variant.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Deleted chromosome 18 with paternal mosaicism

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Constitutional chromosomal breakage

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

A fragile secondary constriction on chromosome 2 in a severely mentally retarded patient

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Familial X-linked mental retardation with an X chromosome abnormality

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Selective endoreduplication or branched chromosome?

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685761

Assignment of aberration breakpoints in banded chromosomes

13 July 2018

1 reference

12 December 2020

Combined mongolism and leukemia. Report of eight cases with chromosome studies

1 reference

12 December 2020

Selective endoreduplication of the long arm of the 2 chromosome in a woman and her daughter

1 reference

12 December 2020

Familial normal/partial trisomy 16 with selective endoreduplication in malformed proband

1 reference

12 December 2020

Heritable Fragile Site on Chromosome 16: Probable Localization of Haptoglobin Locus in Man

1 reference

12 December 2020

Structural Polymorphism in Chromosome 17

1 reference

12 December 2020

Virus as a cause of chromosome aberrations in man

1 reference

12 December 2020

Chromosome abnormality and hypocalcemia in congenital erythroid hypoplasia (blackfan-diamond syndrome)

1 reference

12 December 2020

Persisting clone of cells with an abnormal chromosome in a woman previously irradiated

1 reference

12 December 2020

Identifiers

PMC publication ID

1685761

1 reference

7 August 2017

1 reference