Pancreatic function and gene deletion F508 in cystic fibrosis.
about
Nine cystic fibrosis patients homozygous for the CFTR nonsense mutation R1162X have mild or moderate lung disease.Cystic fibrosis identified by neonatal screening: incidence, genotype, and early natural history.Genotype-phenotype correlation in cystic fibrosis: the role of modifier genes.A very unusual case of hypokalaemia.Early and late outcome of cystic fibrosis screening.
P2860
Pancreatic function and gene deletion F508 in cystic fibrosis.
description
1990 nî lūn-bûn
@nan
1990 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Pancreatic function and gene deletion F508 in cystic fibrosis.
@ast
Pancreatic function and gene deletion F508 in cystic fibrosis.
@en
type
label
Pancreatic function and gene deletion F508 in cystic fibrosis.
@ast
Pancreatic function and gene deletion F508 in cystic fibrosis.
@en
prefLabel
Pancreatic function and gene deletion F508 in cystic fibrosis.
@ast
Pancreatic function and gene deletion F508 in cystic fibrosis.
@en
P2093
P2860
P356
P1476
Pancreatic function and gene deletion F508 in cystic fibrosis.
@en
P2093
P2860
P304
P356
10.1136/JMG.27.11.665
P407
P577
1990-11-01T00:00:00Z