Cranioectodermal dysplasia: a new patient with an inapparent, subtle phenotype. [electronic resource]
Producer: 20011101Description: 332-5 p. digitalISSN:- 0736-8046
- Bone and Bones -- abnormalities
- Child, Preschool
- Craniofacial Abnormalities -- diagnosis
- Ectodermal Dysplasia -- diagnosis
- Female
- Follow-Up Studies
- Hair -- abnormalities
- Hand Deformities, Congenital -- genetics
- Humans
- Italy
- Magnetic Resonance Imaging
- Phenotype
- Syndrome
- Tooth Abnormalities -- diagnosis
No physical items for this record
Publication Type: Case Reports; Journal Article
There are no comments on this title.
Log in to your account to post a comment.