(Q35200473)

7 August 2017

title

Abnormalities in the cell-division cycle in Roberts syndrome fibroblasts: a cellular basis for the phenotypic characteristics? (English)

1 reference

7 August 2017

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D J Tomkins

1

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7 August 2017

J E Sisken

series ordinal

2

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7 August 2017

language of work or name

English

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publication date

1 November 1984

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American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

36

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7 August 2017

issue

6

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7 August 2017

page(s)

1332-1340

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Studies on Down's syndrome in tissue culture. I. Growth rates and protein contents of fibroblast cultures

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=1684655

The SC phocomelia and the Roberts syndrome: nosologic aspects

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684655

Roberts' syndrome.I. Cytological evidence for a disturbance in chromatid pairing

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684655

Cytogenetic findings in Roberts-SC phocomelia syndrome(s)

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684655

The prolongation of mitotic stages in SV40-transformed vs nontransformed human fibroblast 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=1684655

Two children with deletion of the long arm of chromosome 4 with breakpoint at band q33.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684655

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684655

The SC phocomelia syndrome: Report of two cases with cytogenetic abnormality

15 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684655

Systematic growth studies, cocultivation, and cell hybridization studies of Werner syndrome cultured skin fibroblasts

15 November 2018

1 reference

12 December 2020

Differential cell division in human X chromosome mosaics

1 reference

12 December 2020

Comparison of cell cycle time in normal and trisomic cells

1 reference

12 December 2020

The effects of p-DL-fluorophenylalanine on chromosome movement and cytokinesis of human amnion cells in culture

1 reference

12 December 2020

Identifiers

PMC publication ID

1684655

1 reference

7 August 2017

1 reference