(Q35198396)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

title

Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

1 reference

1 reference

Auburger G

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

Diaz GO

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

Capote RF

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

Sanchez SG

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

Perez MP

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

del Cueto ME

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

Meneses MG

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

Farrall M

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

Williamson R

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

Chamberlain S

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

language of work or name

English

0 references

publication date

1 June 1990

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

21 September 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

volume

46

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

page(s)

1163-1177

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

Joseph disease: a multisystem degenerative disorder of the nervous system

21 September 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

A new form of heredo-familial spinocerebellar degeneration with slow eye movements (nine families)

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

The olivopontocerebellar atrophies: a review

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

Genetic homogeneity at the Friedreich ataxia locus on chromosome 9

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

DNA-RFLP analysis and genotyping of HLA-DR and DQ antigens

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

Linkage relationships of the human methylmalonyl CoA mutase to the HLA and D6S4 loci on chromosome 6

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

HLA and complement typing in olivo-ponto-cerebellar atrophy

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

Genetic linkage studies in man

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

Letter: Hereditary ataxia and HL-A genotypes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

Hereditary ataxia and the sixth chromosome

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683834

Serotyping for homotransplantation. 18. Refinement of microdroplet lymphocyte cytotoxicity test

15 November 2018

1 reference

12 December 2020

Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing

1 reference

12 December 2020

A family with hereditary ataxia: HLA typing

1 reference

12 December 2020

A linkage study of hereditary ataxias and related disorders. Evidence of heterogeneity of dominant cerebellar ataxia

1 reference

12 December 2020

Linkage between late onset, dominant spinocerebellar ataxia and HLA

1 reference

12 December 2020

Hereditary cerebellar ataxia and genetic linkage with HLA

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971152%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

PubMed publication ID

1971152

1 reference