[Neonatal screening of cystic fibrosis: diagnostic and ethical problems with mild mutations]
Arch Pediatr
.
2005 Jun;12(6):650-3.
doi: 10.1016/j.arcped.2005.04.063.
[Article in French]
Authors
M Roussey
1
,
A Le Bihannic
,
M P Audrezet
,
M Blayau
,
M Dagorne
,
E Deneuville
,
C Férec
,
H Journel
,
V Moisan-Petit
,
G Rault
,
V Scotet
,
V Storni
,
P Vigneron
Affiliation
1
CRCM de Rennes, institut de la mère et de l'enfant, hôpital Sud-CHU de Rennes, 16, boulevard de Bulgarie, 35203 Rennes, France.
PMID:
15904758
DOI:
10.1016/j.arcped.2005.04.063
No abstract available
MeSH terms
Cystic Fibrosis / diagnosis*
Cystic Fibrosis / genetics*
France
Humans
Infant, Newborn
Mutation*
Neonatal Screening / ethics*