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Mutation in IFT80 in a fetus with the phenotype of Verma-Naumoff provides molecular evidence for Jeune-Verma-Naumoff dysplasia spectrum
Cavalcanti, D. P., Huber, C., Le Quan Sang, K.-H., Baujat, G., Collins, F., Delezoide, A.-L., Dagoneau, N., Le Merrer, M., Martinovic, J., Mello, M. F. S., Vekemans, M., Munnich, A., Cormier-Daire, V.Volume:
48
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmg.2009.069468
Date:
February, 2011
File:
PDF, 240 KB
english, 2011