Format

Send to:

Choose Destination
See comment in PubMed Commons below
J Med Genet. 1980 Dec;17(6):480-3.

Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotype.

Abstract

A patient with a partial deletion (q23 leads to qter) of the long arm of chromosome 11 presented with craniosynostosis and syndactyly. These characteristics, which have not been previously reported with 11q--, expand the phenotype of this syndrome and emphasise the need for chromosome analysis with banding techniques in multiple congenital anomaly syndromes, even if the patient could be classified as having a non-chromosomal syndrome.

PMID:
7205433
[PubMed - indexed for MEDLINE]
PMCID:
PMC1885929
Free PMC Article
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for HighWire Icon for PubMed Central
    Loading ...
    Write to the Help Desk