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1.
Ceylon Med J ; 2002 Dec; 47(4): 139-41
Article in English | IMSEAR | ID: sea-49026
2.
Ceylon Med J ; 2001 Dec; 46(4): 156-7
Article in English | IMSEAR | ID: sea-48802

ABSTRACT

A case of arthrogryposis multiplex congenita distal type II associated with facial abnormality, renal abnormality, postaxial poydactyly and Hirschprung's disease is described. It appears to be a new form of an autosomal recessive disorder.


Subject(s)
Abnormalities, Multiple , Arthrogryposis/pathology , Humans , Infant, Newborn , Male
3.
Ceylon Med J ; 2001 Jun; 46(2): 69-70
Article in English | IMSEAR | ID: sea-47557
7.
Ceylon Med J ; 1976 Sep; 21(3): 183-7
Article in English | IMSEAR | ID: sea-47392
8.
Ceylon Med J ; 1974 Dec; 19(3): 188-91
Article in English | IMSEAR | ID: sea-48478
9.
Ceylon Med J ; 1972 Dec; 17(4): 219-22
Article in English | IMSEAR | ID: sea-48105
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