(Q46221662)

20 December 2017

title

Highly informative dinucleotide repeat polymorphism at the D11S29 locus on chromosome 11q23 (English)

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main subject

human chromosome 11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1601428

13 October 2022

repetitive DNA

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1601428

13 October 2022

1 reference

13 October 2022

1

L. Warnich

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1601428

13 October 2022

author name string

I. Groenewald

2

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L. Theart

3

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A.E. Retief

4

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A. E. Retief

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1601428

13 October 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1601428

13 October 2022

publication date

1 May 1992

1 reference

20 December 2017

full work available at URL

May 1992

0 references

http://link.springer.com/content/pdf/10.1007/BF00220560.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00220560/fulltext.html

13 October 2022

1 reference

http://link.springer.com/content/pdf/10.1007/BF00220560

13 October 2022

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13 October 2022

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20 December 2017

volume

89

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20 December 2017

page(s)

357-359

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20 December 2017

issue

3

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20 December 2017

https://scigraph.springernature.com/pub.10.1007/bf00220560

exact match

0 references

cites work

Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus: exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large kindred

1 reference

12 December 2020

Comparative mapping of the constitutional and tumor-associated 11;22 translocations

1 reference

12 December 2020

An anonymous human single copy genomic clone, D11S29 (L7) at 11q23, identifies a moderately frequent RFLP

1 reference

12 December 2020

Five polymorphic microsatellite VNTRs on the human X chromosome.

1 reference

12 December 2020

Genetic heterogeneity in tuberous sclerosis

1 reference

12 December 2020

Further mapping of an ataxia-telangiectasia locus to the chromosome 11q23 region

1 reference

12 December 2020

Report of the committee on the genetic constitution of chromosome 11.

1 reference

12 December 2020

Report of the committee on the genetic constitution of chromosome 11.

1 reference

12 December 2020

Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms

1 reference

12 December 2020

Analysis of 7 polymorphic markers at chromosome 11q22-23 in 35 ataxia telangiectasia families; further evidence of linkage

1 reference

12 December 2020

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

1 reference

12 December 2020

A detailed genetic map of the long arm of chromosome 11

1 reference

12 December 2020

Mapping of a gene determining tuberous sclerosis to human chromosome 11q14-11q23.

1 reference

12 December 2020

Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms

1 reference

12 December 2020

Report of the committee on structural chromosome changes in neoplasia

1 reference

12 December 2020

A primary linkage map of the human chromosome 11q22-23 region

1 reference

12 December 2020

Localization of an ataxia-telangiectasia gene to chromosome 11q22-23.

1 reference

12 December 2020

Identification of a hypervariable microsatellite polymorphism within D9S15 tightly linked to Friedrich's ataxia

1 reference

12 December 2020

Identifiers

0 references

1 reference

20 December 2017