Behçet's syndrome: a family study and the elucidation of a genetic role
about
Neonatal Behçet's syndrome in an infant of a mother with the diseaseNovel heterozygous C243Y A20/TNFAIP3 gene mutation is responsible for chronic inflammation in autosomal-dominant Behçet's diseaseBehçet's syndrome in pregnancy.Genetic variants in the JAK1 gene confer higher risk of Behcet's disease with ocular involvement in Han Chinese.Identification of an autosomal recessive mode of inheritance in paediatric Behçet's families by segregation analysis.
P2860
Behçet's syndrome: a family study and the elucidation of a genetic role
description
1979 nî lūn-bûn
@nan
1979 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1979 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1979年の論文
@ja
1979年論文
@yue
1979年論文
@zh-hant
1979年論文
@zh-hk
1979年論文
@zh-mo
1979年論文
@zh-tw
1979年论文
@wuu
name
Behçet's syndrome: a family study and the elucidation of a genetic role
@ast
Behçet's syndrome: a family study and the elucidation of a genetic role
@en
Behçet's syndrome: a family study and the elucidation of a genetic role.
@nl
type
label
Behçet's syndrome: a family study and the elucidation of a genetic role
@ast
Behçet's syndrome: a family study and the elucidation of a genetic role
@en
Behçet's syndrome: a family study and the elucidation of a genetic role.
@nl
prefLabel
Behçet's syndrome: a family study and the elucidation of a genetic role
@ast
Behçet's syndrome: a family study and the elucidation of a genetic role
@en
Behçet's syndrome: a family study and the elucidation of a genetic role.
@nl
P2093
P2860
P356
P1476
Behçet's syndrome: a family study and the elucidation of a genetic role
@en
P2093
P2860
P304
P356
10.1136/ARD.38.2.118
P407
P577
1979-04-01T00:00:00Z