CORE
🇺🇦
make metadata, not war
Services
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
A novel menin gene deletional mutation in a little series of Italian patients affected by apparently sporadic multiple endocrine neoplasia type 1 syndrome
Authors
A Cebrián
A Falchetti
+31 more
A Gracanin
A Poisson
AA Pannett
American Society of Clinical Oncology
BT Teh
CA Stratakis
D Trump
F Bosman
GM Doherty
H Raef
I Marinoni
JH Bassett
K Balogh
M Fujimori
M Georgitsi
M Georgitsi
M Kassem
MA Kouvaraki
MC Lemos
MC Lemos
MC Schmidt
ML Brandi
P Ferolla
R Hou
RD Klein
S Marx
SC Chandrasekharappa
SC Chandrasekharappa
SK Agarwal
SS Guo
V Wautot
Publication date
Publisher
'Springer Science and Business Media LLC'
Doi
Cite
Abstract
Abstract is not available.
Similar works
Full text
Available Versions
Crossref
See this paper in CORE
Go to the repository landing page
Download from data provider
info:doi/10.1007%2Fbf03345419
Last time updated on 13/11/2020