Abstract |
A single case of the hypertelorism microtia clefting (HMC) syndrome, a rare autosomal recessive condition, is reported.
|
Authors | M Baraitser |
Journal | Journal of medical genetics
(J Med Genet)
Vol. 19
Issue 5
Pg. 387-8
(Oct 1982)
ISSN: 0022-2593 [Print] England |
PMID | 7143395
(Publication Type: Case Reports, Journal Article)
|
Topics |
- Cleft Lip
(genetics)
- Cleft Palate
(genetics)
- Craniofacial Dysostosis
(genetics)
- Ear, External
(abnormalities)
- Humans
- Hypertelorism
(genetics)
- Infant, Newborn
- Male
- Syndrome
|