(Q33592545)

28 July 2017

Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8) (English)

1 reference

28 July 2017

0 references

Benign hereditary chorea

1 reference

Quarrell OW

1

1 reference

28 July 2017

Youngman S

series ordinal

2

1 reference

28 July 2017

Sarfarazi M

series ordinal

3

1 reference

28 July 2017

Harper PS

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 March 1988

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

25

1 reference

28 July 2017

3

1 reference

28 July 2017

191-194

1 reference

Benign familial chorea: an association with intellectual impairment

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015485

Strategies for multilocus linkage analysis in humans

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015485

Benign (non-paroxysmal) familial chorea. Paediatric perspectives

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015485

A polymorphic DNA marker genetically linked to Huntington's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015485

Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015485

Familial benign chorea with intention tremor: a clinical entity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015485

Studies of a DNA marker (G8) genetically linked to Huntington disease in British families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015485

Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015485

Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015485

Huntington's disease: two families with differing clinical features show linkage to the G8 probe

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015485

Benign hereditary non-progressive chorea of early onset. Clinical genetics of the syndrome and report of a new family

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015485

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015485

Benign hereditary chorea--response to steroids

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2895189

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1015485

1 reference

28 July 2017

1 reference