Trisomy 1q43 syndrome: a consistent phenotype with macrocephaly, characteristic face, developmental delay and cardiac anomalies.

Subjects

Subjects :

UMCN 5.1: Genetic defects of metabolism.

Details

Database :

OAIster

Notes :

Jackson, K.E. author., Tsien, F. author., Marble, M.R. author.

Accession number :

edsoai.on1443332756