Cranioectodermal dysplasia (Sensenbrenner's syndrome)
J Med Genet
.
1989 Jun;26(6):393-6.
doi: 10.1136/jmg.26.6.393.
Author
I D Young
1
Affiliation
1
Department of Child Health, Leicester Royal Infirmary.
PMID:
2661822
PMCID:
PMC1015626
DOI:
10.1136/jmg.26.6.393
No abstract available
Publication types
Case Reports
Review
MeSH terms
Abnormalities, Multiple
Diseases in Twins
Female
Humans
Infant
Male
Skin Abnormalities*
Skull / abnormalities*
Syndrome