1. Adinolfi, M., 1992a, Fetal nucleated cells in the maternal circulation, in: Prenatal Diagnosis and Screening (D.J.H. Brock, C.H. Rodeck, and M.A. Ferguson-Smith, eds.), London pp. 651–662, Churchill Livingstone, Edinburgh.
2. Adinolfi, M., 1992b, Breaking the blood barrier, Nature Genet. 1:316–318.
3. Adinolfi, M., 1993, Hunter syndrome: Cloning of the gene, mutations and carrier detection, Dev. Med. Child Neurol. 35:79–85.
4. Adinolfi, M., and Davies, A.F., 1994, Non-isotopic In Situ Hybridization: Applications to Clinical Diagnosis and Molecular Genetics, RG Landes, Austin, Texas.
5. Adinolfi, M., Davies, A., Sharif, S., Soothill, P., and Rodeck, C., 1993, Detection of trisomy 18 and Y-derived sequences in fetal nucleated cells obtained by transcervical flushing, Lancet 342:403–404.