RT Journal Article
SR Electronic
T1 A new form of autosomal dominant arthrogryposis.
JF Journal of Medical Genetics
JO J Med Genet
FD BMJ Publishing Group Ltd
SP 701
OP 703
DO 10.1136/jmg.28.10.701
VO 28
IS 10
A1 M M Lai
A1 M A Tettenborn
A1 J G Hall
A1 L J Smith
A1 A C Berry
YR 1991
UL http://jmg.bmj.com/content/28/10/701.abstract
AB We report a man and his son with congenital limb contractures, limitation of ocular movements, and an electroretinal abnormality. They appear to have an autosomal dominant form of arthrogryposis, distinguishable from other previously classified forms of this disorder.