Poids de l’Open access dans la production CNRS
Home
Resources
Graphs
Search
Export
Sign in
Titre
Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations
XX
BSO - Titre
Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused byCLDN19gene mutations
XX
DOI
DOI
10.1136/jmedgenet-2016-103956
XX
DOAI
DOAI
10.1136/jmedgenet-2016-103956
XX
Identifiant WoS
WOS:000391458700004
XX
Accès ouvert
OA - Non
XX
Source - Accès ouvert
OA - Non
XX
Type d'accès
Non OA
XX
Editeur
BMJ
XX
Source
JOURNAL OF MEDICAL GENETICS
XX
ISSN
0022-2593
XX
Type de document
Article
XX
Notoriété
4 - Excellente
XX
CNRS
Oui
XX
CNRS - Institut
INSB - Institut des sciences biologiques
XX
uid:/41Z0STW9
12/10/2021 14:52:34 (latest)
Add field
Share/Export
Powered by
Lodex
9.6.0
