(Q59095680)

6 October 2019

title

Mapping of mutation causing Friedreich's ataxia to human chromosome 9 (English)

1 reference

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6 October 2019

1 reference

2

1 reference

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6 October 2019

author name string

Chamberlain S

1

1 reference

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6 October 2019

Rowland A

3

1 reference

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6 October 2019

Wallis J

4

1 reference

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6 October 2019

South S

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

Nakamura Y

6

1 reference

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6 October 2019

von Gabain A

7

1 reference

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6 October 2019

Farrall M

8

1 reference

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6 October 2019

Williamson R

9

1 reference

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6 October 2019

language of work or name

English

0 references

publication date

1 July 1988

1 reference

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6 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

volume

334

1 reference

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6 October 2019

issue

6179

1 reference

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6 October 2019

page(s)

248-250

1 reference

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Clinical Description and Roentgenologic Evaluation of Patients with Friedreich's Ataxia

6 October 2019

cites work

1 reference

7 January 2021

Study of Fatal Cases of Friedreich's Ataxia

1 reference

7 January 2021

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

7 January 2021

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

1 reference

7 January 2021

A polymorphic DNA marker genetically linked to Huntington's disease

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7 January 2021

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

1 reference

7 January 2021

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

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7 January 2021

A closely linked genetic marker for cystic fibrosis

1 reference

7 January 2021

Exclusion of the Friedreich ataxia gene from chromosome 19

1 reference

7 January 2021

Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features

1 reference

7 January 2021

Close linkage of alpha and beta interferons and infrequent duplication of beta interferon in humans

1 reference

7 January 2021

Isolation and mapping of a polymorphic DNA sequence pMCT112 on chromosome 9q (D9S15).

1 reference

7 January 2021

A genetic linkage map of the human genome.

1 reference

7 January 2021

The 1985 human gene map and human gene mapping in 1985

1 reference

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

7 January 2021

Leukocyte and fibroblast interferon genes are located on human chromosome 9

1 reference

7 January 2021

Interferon and c-ets-1 genes in the translocation (9;11)(p22;q23) in human acute monocytic leukemia

1 reference

7 January 2021

Report of the Committee on the Genetic Constitution of Chromosomes 7, 8 and 9

1 reference

7 January 2021

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

1 reference

7 January 2021

Friedreich's ataxia in Kathikas-Arodhes, Cyprus

1 reference

7 January 2021