(Q36414854)

14 August 2017

A fine structure physical map of the short arm of chromosome 5 (English)

1 reference

14 August 2017

J Overhauser

1

1 reference

14 August 2017

A L Beaudet

series ordinal

2

1 reference

14 August 2017

J J Wasmuth

series ordinal

3

1 reference

14 August 2017

language of work or name

English

0 references

publication date

1 November 1986

1 reference

American Journal of Human Genetics

14 August 2017

1 reference

14 August 2017

39

1 reference

14 August 2017

5

1 reference

14 August 2017

562-572

1 reference

Selective linkage disruption in human-Chinese hamster cell hybrids: deletion mapping of the leuS, hexB, emtB, and chr genes on human chromosome 5

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684052

Interstitial deletion of the short arm of chromosome 5 in a mother and three children.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684052

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684052

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684052

Removal of repeated sequences from hybridisation probes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684052

Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684052

Molecular approach to analyzing the human 5p deletion syndrome, cri du chat

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684052

A cell hybrid and recombinant DNA library that facilitate identification of polymorphic loci in the vicinity of the Huntington disease gene

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684052

The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684052

Linkage of the leuS, emtB, and chr genes on chromosome 5 in humans and expression of human genes encoding protein synthetic components in human--Chinese hamster hybrids

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684052

Cytologic observations in 35 individuals with a 5p- karyotype

28 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2878609

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

14 August 2017

PubMed publication ID

2878609

1 reference