On the nosology of the Cornelia de Lange and Coffin-Siris syndromes
Clin Genet
.
1986 Mar;29(3):263-4.
doi: 10.1111/j.1399-0004.1986.tb00824.x.
Author
J P Fryns
PMID:
3698337
DOI:
10.1111/j.1399-0004.1986.tb00824.x
No abstract available
Publication types
Letter
MeSH terms
Abnormalities, Multiple / genetics*
Bone and Bones / abnormalities*
De Lange Syndrome / diagnosis
De Lange Syndrome / genetics*
Diagnosis, Differential
Female
Genes, Dominant
Humans
Syndrome