[Robin's syndrome with hypoplasia of the maxilla and nose--a genetic malformation combination?]
Fortschr Kiefer Gesichtschir
.
1976:21:262-6.
[Article in German]
Authors
J F Kreidler
,
W R Koberg
,
U Kröhne
PMID:
1068063
No abstract available
MeSH terms
Abnormalities, Multiple / genetics*
Adult
Cephalometry
Child
Child, Preschool
Female
Humans
Male
Nose Deformities, Acquired*
Pierre Robin Syndrome / genetics*