(Q36691292)

English

Investigations with fluorescence in situ hybridization (FISH) demonstrate loss of the telomeres on the reciprocal chromosome in three unbalanced translocations involving chromosome 15 in the Prader-Willi and Angelman syndromes

scientific article published on September 1, 1995

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

Investigations with fluorescence in situ hybridization (FISH) demonstrate loss of the telomeres on the reciprocal chromosome in three unbalanced translocations involving chromosome 15 in the Prader-Willi and Angelman syndromes (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

author name string

A. Jauch

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7649555

16 July 2024

L. Robson

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7649555

16 July 2024

A. Smith

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7649555

16 July 2024

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7649555

16 July 2024

publication date

1 September 1995

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF00210421.pdf

1 reference

10.1007/BF00210421

https://api.crossref.org/works/10.1007/BF00210421

16 July 2024

http://link.springer.com/article/10.1007/BF00210421/fulltext.html

1 reference

10.1007/BF00210421

https://api.crossref.org/works/10.1007/BF00210421

16 July 2024

http://link.springer.com/content/pdf/10.1007/BF00210421

1 reference

10.1007/BF00210421

https://api.crossref.org/works/10.1007/BF00210421

16 July 2024

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

96

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

345-349

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

describes a project that uses

fluorescence in situ hybridization

1 reference

based on heuristic

inferred from title

Post-mortem studies on two patients with 1-2 band cytogenetic deletions: 10q26----qter and r(9)(p24q34)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A severely retarded male with deletion of chromosomes 15 (pter leads to q13) and 10 (q 26 leads to qter)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The presence of interstitial telomeric sequences in constitutional chromosome abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An unusually large (CA)n repeat in the region of divergence between subtelomeric alleles of human chromosome 16p.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Terminal chromosome attachments

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome: current understanding of cause and diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial unbalanced translocation t(8;15)(p23.3;q11) with uniparental disomy in Angelman syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metaphase and interphase cytogenetics with Alu-PCR-amplified yeast artificial chromosome clones containing the BCR gene and the protooncogenes c-raf-1, c-fms, and c-erbB-2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

True telomeric translocation in a baby with the Prader-Willi phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Minireview: cryptic translocations and telomere integrity

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15

1 reference

https://pubmed.ncbi.nlm.nih.gov/7649555

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00210421

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q36691292&oldid=2205465169"