Format

Send to

Choose Destination
See comment in PubMed Commons below
Clin Genet. 1998 Jan;53(1):70-3.

The 4q-syndrome: delineation of the minimal critical region to within band 4q31.

Author information

  • 1Victorian Clinical Genetics Service, Royal Children's Hospital, Parkville, Victoria, Australia.

Abstract

A consistent phenotype has been associated with deletion of the distal long arm of chromosome 4. An invariant requirement for the phenotype in cases described so far has been the deletion of material from within band 4q31 but few other cases have been described that further aid the delineation of the minimum critical region sufficient for the expression of the phenotype. We report a child with a small interstitial deletion within band 4q31 who exhibits most of the features of the established 4q-phenotype.

PMID:
9550366
[PubMed - indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Wiley
    Loading ...
    Support Center