Ontology highlight
ABSTRACT:
SUBMITTER: Bongers EM
PROVIDER: S-EPMC1182087 | biostudies-literature | 2004 Jun
REPOSITORIES: biostudies-literature
Bongers Ernie M H F EM Duijf Pascal H G PH van Beersum Sylvia E M SE Schoots Jeroen J Van Kampen Albert A Burckhardt Andreas A Hamel Ben C J BC Losan Frantisek F Hoefsloot Lies H LH Yntema Helger G HG Knoers Nine V A M NV van Bokhoven Hans H
American journal of human genetics 20040421 6
Small patella syndrome (SPS) is an autosomal-dominant skeletal dysplasia characterized by patellar aplasia or hypoplasia and by anomalies of the pelvis and feet, including disrupted ossification of the ischia and inferior pubic rami. We identified an SPS critical region of 5.6 cM on chromosome 17q22 by haplotype analysis. Putative loss-of-function mutations were found in a positional gene encoding T-box protein 4 (TBX4) in six families with SPS. TBX4 encodes a transcription factor with a strongl ...[more]