(Q37392695)

English

Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps

scientific article published on August 1986

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

20 August 2017

Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps (English)

1 reference

Europe PubMed Central

20 August 2017

author name string

H F Willard

1

1 reference

Europe PubMed Central

20 August 2017

J S Waye

2

1 reference

Europe PubMed Central

20 August 2017

M H Skolnick

3

1 reference

Europe PubMed Central

20 August 2017

C E Schwartz

4

1 reference

Europe PubMed Central

20 August 2017

V E Powers

5

1 reference

Europe PubMed Central

20 August 2017

S B England

6

1 reference

Europe PubMed Central

20 August 2017

language of work or name

0 references

publication date

1 August 1986

1 reference

Europe PubMed Central

20 August 2017

number of pages

5

1 reference

based on heuristic

inferred from page(s)

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

20 August 2017

83

1 reference

Europe PubMed Central

20 August 2017

15

1 reference

Europe PubMed Central

20 August 2017

5611-5615

1 reference

Europe PubMed Central

20 August 2017

Characterization of a cloned repetitive DNA sequence concentrated on the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

6 September 2017

Characterization of a cloned DNA sequence that is present at centromeres of all human autosomes and the X chromosome and shows polymorphic variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

6 September 2017

A polymorphic DNA marker genetically linked to Huntington's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

6 September 2017

Isolation and characterization of a major tandem repeat family from the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

6 September 2017

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

6 September 2017

The Formation, Structure, and Composition of the Mammalian Kinetochore and Kinetochore Fiber

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

6 September 2017

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

6 September 2017

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

6 September 2017

Linkage map of the short arm of human chromosome 11: location of the genes for catalase, calcitonin, and insulin-like growth factor II.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

6 September 2017

Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

6 September 2017

Recent amplification of an alpha satellite DNA in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

6 September 2017

Chromosomal localization of complex and simple repeated human DNAs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

6 September 2017

Homology between human and simian repeated DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

14 September 2017

The Wilhelmine E. Key 1979 Invitational Lecture: The anatomy of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

14 September 2017

The molecular structure of centromeres and telomeres

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

14 September 2017

A new era in mammalian gene mapping: somatic cell genetics and recombinant DNA methodologies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

14 September 2017

Sequence heterogeneity within the human alphoid repetitive DNA family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

14 September 2017

Chromosome-specific organization of human alpha satellite DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

14 September 2017

The genetic linkage map of the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

26 June 2018

Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

26 June 2018

A cloned sequence, p82H, of the alphoid repeated DNA family found at the centromeres of all human chromosomes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

26 June 2018

Construction of linkage maps with DNA markers for human chromosomes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

26 June 2018

Human chromosome heteromorphisms (variants).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

26 June 2018

DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=386338

26 June 2018

Unequal crossover and the evolution of multigene families

1 reference

https://pubmed.ncbi.nlm.nih.gov/3016709

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long range periodicities in mouse satellite DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/3016709

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3016709

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3016709

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

1 reference

https://pubmed.ncbi.nlm.nih.gov/3016709

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/3016709

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

https://pubmed.ncbi.nlm.nih.gov/3016709

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A closely linked genetic marker for cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3016709

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of cystic fibrosis locus to human chromosome 7cen–q22

1 reference

https://pubmed.ncbi.nlm.nih.gov/3016709

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.83.15.5611

1 reference

Europe PubMed Central

20 August 2017

1986PNAS...83.5611W

0 references

1 reference

Europe PubMed Central

20 August 2017

1 reference

Europe PubMed Central

20 August 2017

ResearchGate publication ID

0 references

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=Q37392695&oldid=2015085525"