CHARACTERIZING THE BASIC GENETIC DEFECT IN WOLF-HIRSCHHORN SYNDROME WITH RESPECT TO PHENOTIPIC IMPLICATIONS
- 2 Years 2004/2006
- 99.000€ Total Award
The relevance of this project is related to: 1)proper diagnostic protocol and counseling in WHS; 2) definition of additional, currently unkown, genetic factors that account for the final phenotype; 3)clarify the role of the common inversion polymorphisms in generating common genomic rearrangements; 4)improve the general knowledge of WHS.
