Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome.

Subjects

Subjects :

UMCN 5.1: Genetic defects of metabolism.
UMCN 5.3: Cellular energy metabolism.

Details

Database :

OAIster

Notes :

Czako, M. author., Karteszi, J. author., Cser, B. author., Weissbecker, K. author., Mehes, K. author.

Accession number :

edsoai.on1443368323