arthrogryposis

n.

关节挛缩；

ARTHROGRYPOSIS MULTIPLEX DUE TO CONGENITAL MUSCULAR DYSTROPHY1
EXPERIMENTAL CLUBFOOT AND ARTHROGRYPOSIS MULTIPLEX CONGENITA
Arthrogryposis multiplex congenita: etiology, genetics, classification, diagnostic approach, and general aspects
Association of arthrogryposis multiplex congenita with maternal antibodies inhibiting fetal acetylcholine receptor function.
Teratogen update: maternal myasthenia gravis as a cause of congenital arthrogryposis
Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes.
Corrigendum: Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithe...
Mutations in TNNT3 cause multiple congenital contractures: a second locus for distal arthrogryposis type 2B.
Riemersma, S. et al. Association of arthrogryposis multiplex congenita with maternal antibodies inhibiting fetal acetylcholine-recep...
Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis|[ndash]|renal dysfunction|[ndash]...