(Q77359298)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11746047%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

title

Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qter (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11746047%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

author name string

M G Tanamy

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11746047%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

N Magal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11746047%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

G J Halpern

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11746047%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

L Jaber

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11746047%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

M Shohat

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11746047%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

publication date

1 November 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11746047%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics Part A

5 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11746047%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

volume

104

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11746047%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

issue

2

1 reference

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5 December 2019

page(s)

152-156

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11746047%20AND%20SRC:MED&resulttype=core&format=json

Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association

5 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10030

Molecular cloning and expression of the gene for a human D1 dopamine receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10030

Arthrogryposis multiplex congenita in an Arab kindred: update

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10030

Identification of two distinct synucleins from human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10030

Identification of high-molecular-weight proteins with multiple EGF-like motifs by motif-trap screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10030

A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10030

Assignment of human alpha-synuclein (SNCA) and beta-synuclein (SNCB) genes to chromosomes 4q21 and 5q35.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10030

Dopamine D1 receptor mutant mice are deficient in striatal expression of dynorphin and in dopamine-mediated behavioral responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10030

21 January 2018

Identifiers

DOI

10.1002/AJMG.10030

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11746047%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

1 reference