Congenital heart defects common in rhizomelic chondrodysplasia punctata. [electronic resource]
- American journal of medical genetics. Part A Jan 2016
- 270-2 p. digital
Publication Type: Letter; Research Support, Non-U.S. Gov't
1552-4833
10.1002/ajmg.a.37404 doi
Acyltransferases--genetics Child Child, Preschool Chondrodysplasia Punctata, Rhizomelic--genetics Female Heart Defects, Congenital--epidemiology Humans Infant Male Peroxisomal Targeting Signal 2 Receptor Peroxisomes--pathology Receptors, Cytoplasmic and Nuclear--genetics