RT Journal Article
SR Electronic
T1 A case of Fryns syndrome.
JF Journal of Medical Genetics
JO J Med Genet
FD BMJ Publishing Group Ltd
SP 82
OP 84
DO 10.1136/jmg.23.1.82
VO 23
IS 1
A1 Young, I D
A1 Simpson, K
A1 Winter, R M
YR 1986
UL http://jmg.bmj.com/content/23/1/82.abstract
AB A case of Fryns syndrome is presented. Characteristic features of this lethal autosomal recessive disorder include corneal clouding, camptodactyly with hypoplastic nails, and abnormalities of the diaphragm.