Restoring old revision of "Q28142532"

Jump to navigation Jump to search

Warning: You are not logged in. Your IP address will be publicly visible if you make any edits. If you log in or create an account, your edits will be attributed to a username, among other benefits.

Latest revision
Your text
label / astlabel / ast
Bethlem myopathy: a slowly progressive congenital muscular dystrophy with contractures
description / hydescription / hy
1999 թվականի ապրիլին հրատարակված գիտական հոդված
գիտական հոդված
description / ukdescription / uk
наукова стаття, опублікована у квітні 1999
наукова стаття
description / astdescription / ast
artículu científicu espublizáu en 1999
artículu científicu
description / hywdescription / hyw
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
Property / volume
122
 
Property / volume: 122 / rank
Normal rank
 
Property / page(s)
649-655
 
Property / page(s): 649-655 / rank
Normal rank
 
Property / author name string
G. J. Jöbsis
 
Property / author name string: G. J. Jöbsis / rank
Normal rank
 
Property / author name string: G. J. Jöbsis / qualifier
 
Property / author name string
J. M. Boers
 
Property / author name string: J. M. Boers / rank
Normal rank
 
Property / author name string: J. M. Boers / qualifier
 
Property / author name string
P. G. Barth
 
Property / author name string: P. G. Barth / rank
Normal rank
 
Property / author name string: P. G. Barth / qualifier
 
Property / author name string
M. de Visser
 
Property / author name string: M. de Visser / rank
Normal rank
 
Property / author name string: M. de Visser / qualifier
 
Property / main subject
 
Property / main subject: Bethlem myopathy / rank
Normal rank
 
Property / main subject: Bethlem myopathy / reference
 
Property / DOI
 
Property / DOI: 10.1093/BRAIN/122.4.649 / rank
Normal rank
 
Property / issue
4
 
Property / issue: 4 / rank
Normal rank
 
Property / cites work
 
Property / cites work: Further investigations on benign myopathy with autosomal dominant inheritance / rank
Normal rank
 
Property / cites work: Further investigations on benign myopathy with autosomal dominant inheritance / reference
stated in: Crossref
reference URL: https://api.crossref.org/works/10.1093%2FBRAIN%2F122.4.649
retrieved: 21 January 2018
Timestamp+2018-01-21T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
 
Property / cites work
 
Property / cites work: Benign myopathy, with autosomal dominant inheritance. A report on three pedigrees / rank
Normal rank
 
Property / cites work: Benign myopathy, with autosomal dominant inheritance. A report on three pedigrees / reference
stated in: Crossref
reference URL: https://api.crossref.org/works/10.1093%2FBRAIN%2F122.4.649
retrieved: 21 January 2018
Timestamp+2018-01-21T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
 
Property / cites work
 
Property / cites work: Structural and functional features of the alpha 3 chain indicate a bridging role for chicken collagen VI in connective tissues / rank
Normal rank
 
Property / cites work: Structural and functional features of the alpha 3 chain indicate a bridging role for chicken collagen VI in connective tissues / reference
stated in: Crossref
reference URL: https://api.crossref.org/works/10.1093%2FBRAIN%2F122.4.649
retrieved: 21 January 2018
Timestamp+2018-01-21T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
 
Property / cites work
 
Property / cites work: Genetic localization of Bethlem myopathy / rank
Normal rank
 
Property / cites work: Genetic localization of Bethlem myopathy / reference
stated in: Crossref
reference URL: https://api.crossref.org/works/10.1093%2FBRAIN%2F122.4.649
retrieved: 21 January 2018
Timestamp+2018-01-21T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
 
Property / cites work
 
Property / cites work: Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures / rank
Normal rank
 
Property / cites work: Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures / reference
stated in: Crossref
reference URL: https://api.crossref.org/works/10.1093%2FBRAIN%2F122.4.649
retrieved: 21 January 2018
Timestamp+2018-01-21T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
 
Property / cites work
 
Property / cites work: A Danish family with limb-girdle muscular dystrophy with autosomal dominant inheritance / rank
Normal rank
 
Property / cites work: A Danish family with limb-girdle muscular dystrophy with autosomal dominant inheritance / reference
stated in: Crossref
reference URL: https://api.crossref.org/works/10.1093%2FBRAIN%2F122.4.649
retrieved: 21 January 2018
Timestamp+2018-01-21T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
 
Property / cites work
 
Property / cites work: Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI) collagen gene (COL6A3) in a family with Bethlem myopathy / rank
Normal rank
 
Property / cites work: Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI) collagen gene (COL6A3) in a family with Bethlem myopathy / reference
stated in: Crossref
reference URL: https://api.crossref.org/works/10.1093%2FBRAIN%2F122.4.649
retrieved: 21 January 2018
Timestamp+2018-01-21T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
 
Property / cites work
 
Property / cites work: Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin beta 1? / rank
Normal rank
 
Property / cites work: Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin beta 1? / reference
stated in: Crossref
reference URL: https://api.crossref.org/works/10.1093%2FBRAIN%2F122.4.649
retrieved: 21 January 2018
Timestamp+2018-01-21T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
 
Property / cites work
 
Property / cites work: Bethlem myopathy: Early-onset benign autosomal dominant myopathy with contractures. Description of two new families / rank
Normal rank
 
Property / cites work: Bethlem myopathy: Early-onset benign autosomal dominant myopathy with contractures. Description of two new families / reference
stated in: Crossref
reference URL: https://api.crossref.org/works/10.1093%2FBRAIN%2F122.4.649
retrieved: 21 January 2018
Timestamp+2018-01-21T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
 
Property / cites work
 
Property / cites work: Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37 / rank
Normal rank
 
Property / cites work: Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37 / reference
stated in: Crossref
reference URL: https://api.crossref.org/works/10.1093%2FBRAIN%2F122.4.649
retrieved: 21 January 2018
Timestamp+2018-01-21T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
 
Property / ResearchGate publication ID
 
Property / ResearchGate publication ID: 274415380 / rank
Normal rank
 

Cancel
Retrieved from "https://www.wikidata.org/wiki/Q28142532"