(Q57970958)

8

object named as

Y. Agid

0 references

H. Ouhabi

4

object named as

H. Ouhabi

0 references

author name string

A. Benomar

1

0 references

E. Le Guern

2

0 references

A. Dürr

3

0 references

M. Yahyaoui

6

0 references

T. Chkili

7

0 references

A. Brice

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

9

0 references

publication date

April 1994

0 references

published in

Annals of Neurology

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volume

35

0 references

issue

4

0 references

page(s)

439-444

0 references

cites work

1 reference

https://api.crossref.org/works/10.1002%2FANA.410350411

Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410350411

Autosomal dominant retinitis pigmentosa: a mutation in codon 178 of the rhodopsin gene in two families of Celtic origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410350411

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410350411

A simple salting out procedure for extracting DNA from human nucleated cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410350411

A second-generation linkage map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410350411

A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410350411

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410350411

Severity of X-linked recessive bulbospinal neuronopathy correlates with size of the tandem CAG repeat in androgen receptor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410350411

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410350411

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410350411