(Q35198875)

English

Chromatid repulsion associated with Roberts/SC phocomelia syndrome is reduced in malignant cells and not expressed in interspecies somatic-cell hybrids

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3788975%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

Chromatid repulsion associated with Roberts/SC phocomelia syndrome is reduced in malignant cells and not expressed in interspecies somatic-cell hybrids (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3788975%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

author name string

N E Krassikoff

1

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Europe PubMed Central

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4 October 2019

J M Cowan

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3788975%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

D M Parry

3

1 reference

Europe PubMed Central

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4 October 2019

U Francke

4

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Europe PubMed Central

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4 October 2019

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publication date

1 November 1986

1 reference

Europe PubMed Central

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4 October 2019

American Journal of Human Genetics

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Europe PubMed Central

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4 October 2019

39

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4 October 2019

5

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Europe PubMed Central

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4 October 2019

618-630

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Europe PubMed Central

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4 October 2019

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684051

28 July 2018

Isolation and Analysis of Somatic Hybrids Derived from Two Human Diploid Cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684051

28 July 2018

SC phocomelia syndrome, premature centromere separation, and congenital cranial nerve paralysis in two sisters, one with malignant melanoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684051

28 July 2018

The SC phocomelia and the Roberts syndrome: nosologic aspects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684051

28 July 2018

Quantitative analysis of high-resolution trypsin-giemsa bands on human prometaphase chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684051

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684051

28 July 2018

Cytogenetic findings in Roberts-SC phocomelia syndrome(s)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684051

28 July 2018

SELECTION OF HYBRIDS FROM MATINGS OF FIBROBLASTS IN VITRO AND THEIR PRESUMED RECOMBINANTS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684051

26 September 2018

The nuclear envelope lamina is reversibly depolymerized during mitosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684051

26 September 2018

Roberts syndrome: clinical and cytogenetic aspects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684051

26 September 2018

Oligosyndactyly: a lethal mutation in the mouse that results in mitotic arrest very early in development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684051

15 November 2018

Premature centromere splitting in a presumptive mild form of Roberts syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3788975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Roberts syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3788975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Roberts's syndrome. II. Aberrant Y-chromosome behavior

1 reference

https://pubmed.ncbi.nlm.nih.gov/3788975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Four siblings with Robert's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3788975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A dominantly inherited cytogenetic anomaly: a possible cell division mutant

1 reference

https://pubmed.ncbi.nlm.nih.gov/3788975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3788975%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3788975%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

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