CORE
🇺🇦Â
 make metadata, not war
Services
Research
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
Filters
3 research outputs found
Molecular genetic diagnosis of the 1.5Mb deletion causing hereditary neuropathy with liability to pressure palsies (HNPP) in a Polish family
Author
Fidzianska A.
Hausmanowa-Petrusewicz I.
+6Â more
J\ueadrzejowska H.
Kocha\uf1ski A.
L\uf6fgren Ann
Latos-Biele\uf1ska A.
Timmerman Vincent
Van Broeckhoven Christine
Publication venue
Publication date
01/01/1999
Field of study
No full text
Biblioteka Nauki - repozytorium artykułów
Institutional Repository Universiteit Antwerpen
A novel connexin 32 missense mutation (E208G) causing Charcot-Marie-Tooth disease
Author
Barciszewska A.
Czarny-Ratajczak M.
+9Â more
De Jonghe Peter
Hausmanowa-Petrusewicz I.
J\ueadrzejowska H.
Kocha\uf1ski A.
L\uf6fgren Ann
Latos-Biele\uf1ska A.
Ryniewicz B.
Samocko J.
Timmerman Vincent
Publication venue
Publication date
01/01/2001
Field of study
No full text
Institutional Repository Universiteit Antwerpen
Mutation screening of Charcot-Marie-Tooth patients in Poland
Author
De Vriendt Els
Hausmanowa-Petrusewicz I.
+8Â more
J\ueadrzejowska H.
Kocha\uf1ski A.
L\uf6fgren Ann
Latos-Biele\uf1ska A.
Ryniewicz B.
Timmerman Vincent
Van Broeckhoven Christine
Wouters V.
Publication venue
Publication date
01/01/1999
Field of study
No full text
Institutional Repository Universiteit Antwerpen
No full text
