D.J. Wilkin
Medical Genetics Branch
National Human Genome Research Institute
National Institutes of Health
Bethesda
USA
Name/email consistency: high
- Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosome. Wilkin, D.J., Szabo, J.K., Cameron, R., Henderson, S., Bellus, G.A., Mack, M.L., Kaitila, I., Loughlin, J., Munnich, A., Sykes, B., Bonaventure, J., Francomano, C.A. Am. J. Hum. Genet. (1998)