XK aprosencephaly may be a new mutation or a dominant genetic defect
Am J Med Genet
.
1989 Oct;34(2):250-1.
doi: 10.1002/ajmg.1320340224.
Author
P J Benke
PMID:
2817005
DOI:
10.1002/ajmg.1320340224
No abstract available
Publication types
Letter
MeSH terms
Brain / abnormalities*
Facial Bones / abnormalities*
Genes, Dominant*
Humans
Mutation*
Syndrome