Human homologues of Osr1 and Osr2 are not involved in a syndrome with distal limb deficiencies, oral abnormalities, and renal defects
- 19 June 2002
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 111 (4) , 455-456
- https://doi.org/10.1002/ajmg.10583
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Osr2, a new mouse gene related to Drosophila odd-skipped, exhibits dynamic expression patterns during craniofacial, limb, and kidney developmentMechanisms of Development, 2001
- Distal limb deficiencies, oral involvement, and renal defect: Report of a third patient and confirmation of a distinct entityAmerican Journal of Medical Genetics, 2000
- Cloning and expression analysis of a mouse gene related to Drosophila odd-skippedMechanisms of Development, 1999
- Dynamic changes in the functions of Odd-skipped during early Drosophila embryogenesisDevelopment, 1998
- Comparison of the Structure and Expression of odd-skipped and Two Related Genes That Encode a New Family of Zinc Finger Proteins in DrosophilaGenetics, 1996
- Basic local alignment search toolJournal of Molecular Biology, 1990
- Apparently new autosomal recessive syndrome of mental retardation, distal limb deficiencies, oral involvement, and possible renal defectAmerican Journal of Medical Genetics, 1987