(Q67482921)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

title

The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

Charcot-Marie-Tooth disease type 1A

13 September 2019

main subject

1 reference

7

Stanton VP Jr

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1303229

11 September 2022

author name string

Valentijn LJ

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Bolhuis PA

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Zorn I

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Hoogendijk JE

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

van den Bosch N

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Hensels GW

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Housman DE

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Fischbeck KH

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Ross DA

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1303229

11 September 2022

publication date

1 June 1992

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

volume

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

page(s)

166-170

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/ng0692-166

13 September 2019

exact match

0 references

cites work

Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc? receptor gene region

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

De-novo mutation in hereditary motor and sensory neuropathy type I.

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

Trembler mouse carries a point mutation in a myelin gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

Genes specifically expressed at growth arrest of mammalian cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

A growth arrest-specific (gas) gene codes for a membrane protein

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

A myelin protein is encoded by the homologue of a growth arrest-specific gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

Direct assignment of the human beta B2 and beta B3 crystallin genes to 22q11.2----q12: markers for neurofibromatosis 2

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

Two new mutants, ‘trembler’ and ‘reeler’, with neurological actions in the house mouse (Mus musculus L.)

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

A dominant control region from the human beta-globin locus conferring integration site-independent gene expression

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

Separation of chromosomal DNA molecules from yeast by orthogonal-field-alternation gel electrophoresis

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

Separation of large DNA molecules by contour-clamped homogeneous electric fields

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-166

7 January 2021

Identifiers

DOI

10.1038/NG0692-166

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303229%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

1 reference