The autosomal recessive form of CMT disease linked to 5q31-q33. (Q39035900)

8 September 2017

title

The autosomal recessive form of CMT disease linked to 5q31-q33. (English)

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8 September 2017

Guilbot A

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8 September 2017

Kessali M

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8 September 2017

Ravisé N

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8 September 2017

Hammadouche T

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8 September 2017

Bouhouche A

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8 September 2017

Maisonobe T

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8 September 2017

Grid D

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8 September 2017

Brice A

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8 September 2017

LeGuern E

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8 September 2017

language of work or name

English

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publication date

1 September 1999

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Annals of the New York Academy of Sciences

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inferred from page(s)

published in

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8 September 2017

volume

883

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8 September 2017

page(s)

453-456

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Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.

8 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08608.X

Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08608.X

Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08608.X

A physical map of 15 loci on human chromosome 5q23-q33 by two-color fluorescence in situ hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08608.X

A YAC contig of approximately 3 Mb from human chromosome 5q31-->q33.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08608.X

A comprehensive genetic map of the human genome based on 5,264 microsatellites

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08608.X

Molecular cloning, sequencing and expression of the mRNA encoding human Cdx1 and Cdx2 homeobox. Down-regulation of Cdx1 and Cdx2 mRNA expression during colorectal carcinogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08608.X

Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08608.X

Disruption of the murine homeobox gene Cdx1 affects axial skeletal identities by altering the mesodermal expression domains of Hox genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08608.X

Physical and Genetic Mapping of the CMT4A Locus and Exclusion of PMP-2 as the Defect in CMT4A

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08608.X

Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08608.X

10.1111/J.1749-6632.1999.TB08608.X

21 January 2018

Identifiers

DOI

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8 September 2017

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