GOMBO syndrome of growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia: a possible "new" recessively inherited MCA/MR syndrome
Am J Med Genet
.
1989 Jan;32(1):15-8.
doi: 10.1002/ajmg.1320320104.
Authors
A Verloes
1
,
J Delfortrie
,
C Lambotte
Affiliation
1
Department of Paediatrics and Human Genetics, Liège State University, Belgium.
PMID:
2705477
DOI:
10.1002/ajmg.1320320104
No abstract available
Publication types
Case Reports
MeSH terms
Abnormalities, Multiple / genetics*
Child
Female
Fingers / abnormalities*
Growth Disorders / genetics*
Humans
Intellectual Disability / genetics*
Male
Microcephaly / genetics*
Microphthalmos / genetics*
Syndrome