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Diagnosis and prevention of fragile-X syndrome. From the family study to the population screening programme: eighteen years of activity.
Giovannucci Uzielli ML, Guarducci S, Cecconi A, Lenzi S, Ricci U, Balestrieri C, Petrocelli P, Lapi E. Giovannucci Uzielli ML, et al. Among authors: guarducci s. Acta Genet Med Gemellol (Roma). 1996;45(1-2):303-8. doi: 10.1017/s0001566000001537. Acta Genet Med Gemellol (Roma). 1996. PMID: 8872054 No abstract available.
Spectrum and distribution of MECP2 mutations in 64 Italian Rett syndrome girls: tentative genotype/phenotype correlation.
Giunti L, Pelagatti S, Lazzerini V, Guarducci S, Lapi E, Coviello S, Cecconi A, Ombroni L, Andreucci E, Sani I, Brusaferri A, Lasagni A, Ricotti G, Giometto B, Nicolao P, Gasparini P, Granatiero M, Uzielli ML. Giunti L, et al. Among authors: guarducci s. Brain Dev. 2001 Dec;23 Suppl 1:S242-5. doi: 10.1016/s0387-7604(01)00342-4. Brain Dev. 2001. PMID: 11738883
Infrared fluorescent automated detection of thirteen short tandem repeat polymorphisms and one gender-determining system of the CODIS core system.
Ricci U, Sani I, Guarducci S, Biondi C, Pelagatti S, Lazzerini V, Brusaferri A, Lapini M, Andreucci E, Giunti L, Giovannucci Uzielli ML. Ricci U, et al. Among authors: guarducci s. Electrophoresis. 2000 Nov;21(17):3564-70. doi: 10.1002/1522-2683(200011)21:17<3564::AID-ELPS3564>3.0.CO;2-O. Electrophoresis. 2000. PMID: 11271472
23 results