Please use this identifier to cite or link to this item:
|Title:||Interstitial deletion of 13q22→q31: Case report and review of the literature|
|Abstract:||In the present study we describe a patient with characteristic brachydactily, developmental delay and interstitial del 13q22→q31. After the review of the literature, few cases sharing similar chromosomal deletions were found and they displayed little resemblance with our patient. We discuss the phenotype correlation among the deleted regions in such cases. © 2006 Lippincott Williams & Wilkins, Inc.|
|Appears in Collections:||Producción científica UdeG (prueba)|
Files in This Item:
There are no files associated with this item.
Items in RIUdeG are protected by copyright, with all rights reserved, unless otherwise indicated.