(Q41536160)

English

Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instability.

scientific article published on August 1993

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scholarly article

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30 October 2019

Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instability (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8365723%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

Orsetta Zuffardi

7

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30 October 2019

author name string

A Pezzolo

1

1 reference

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30 October 2019

G Gimelli

2

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30 October 2019

A Cohen

3

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30 October 2019

A Lavaggetto

4

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30 October 2019

C Romano

5

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30 October 2019

G Fogu

6

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30 October 2019

publication date

1 August 1993

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30 October 2019

1 reference

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30 October 2019

92

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30 October 2019

23-27

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30 October 2019

1

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30 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00216140

0 references

The presence of interstitial telomeric sequences in constitutional chromosome abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Does "ring syndrome" exist? An analysis of 207 case reports on patients with a ring autosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ring chromosome 16: a new case

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cytogenetic and clinical implications of a ring chromosome 2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure and polymorphism of human telomere-associated DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Telomeric associations in a lymphoblastoid cell line from a patient with B-cell follicular lymphoma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Investigation of three patients with the "ring syndrome", including familial transmission of ring 5, and estimation of reproductive risks

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22p.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ring chromosome and latent centromeres

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pigmentary dysplasias and chromosomal mosaicism: report of 9 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human telomeres: fusion and interstitial sites.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A highly conserved repetitive DNA sequence, (TTAGGG)n, present at the telomeres of human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origin of human chromosome 2: an ancestral telomere-telomere fusion

1 reference

https://pubmed.ncbi.nlm.nih.gov/8365723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00216140

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8365723%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

Dimensions Publication ID

0 references

1 reference

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8365723%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

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