A fast, easy and reliable method for hamstrings graft size prediction in anterior cruciate ligament reconstruction von Minoli, C., Travi, M., Monti, C., Ferrua, P., Puce, Marco, Radaelli, S., Menon, A., Tassi, A. L., Randelli, P. S.

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Adaptability and Comparative Biology of Fall Armyworm on Maize and Perennial Forage Species and Relation with Chemical-Bromatological Composition von Ribeiro, L. P., Klock, A. L. S., Nesi, C. N., Luczkievicz, F. R. G., Travi, M. R. L., Rech, A. F.

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New report of a familial case of Moebius syndrome presenting skeletal findings von Graziadio, Carla, Lorenzen, Marina B., Rosa, Rafael F.M., Pinto, Louise L.C., Zen, Paulo R.G., Travi, Giovanni M., Valiatti, Fabiana, Paskulin, Giorgio A.

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Intrafamilial clinical variability in four families with incontinentia pigmenti von Mariath, Luiza M., Santa Maria, Fernanda D., Poziomczyk, Cláudia S., Travi, Giovanni M., Wachholz, Gabriela E., De Souza, Stephanie R., Kiszewski, Ana E., Schuler‐Faccini, Lavínia

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Feasibility Study for a Microchip-Based Approach for Noninvasive Prenatal Diagnosis of Genetic Diseases von CREMONESI, L, GALBIATI, S, FOGLIENI, B, SMID, M, GAMBINI, D, FERRARI, A, VIORA, E, CAMPOGRANDE, M, PAGLIANO, M, TRAVI, M, PIGA, A, RESTAGNO, G, FERRARI, M

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Poland syndrome associated with an aberrant subclavian artery and vascular abnormalities of the retina in a child exposed to misoprostol during pregnancy von Rosa, Rafael Fabiano Machado, Travi, Giovanni M., Valiatti, Fabiana, Zen, Paulo Ricardo Gazzola, Pinto, Louise Lapagesse, Kiss, Andrea, Graziadio, Carla, Paskulin, Giorgio Adriano

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Trisomy 18 and eye anomalies von Correia, Jamile D., da Rosa, Ernani B., Silveira, Daniélle B., Correia, Elisa P. E., Lorenzen, Marina B., Travi, Giovanni M., Rosa, Rosana C. M., Zen, Paulo R. G., Zen, Tatiana D., Rosa, Rafael F. M.

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Visual Outcome and Success of Amblyopia Treatment in Unilateral Small Posterior Lens Opacities and Lenticonus Initially Treated Nonsurgically von Travi, Giovanni M., Schnall, Bruce M., Lehman, Sharon S., Kelly, Christopher J., Hug, Denise, Hirakata, Vânia N., Calhoun, Joseph H.

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β-Thalassemia microelectronic chip: A fast and accurate method for mutation detection von FOGLIENI, Barbara, CREMONESI, Laura, TRAVI, Maurizio, RAVANI, Anna, GIAMBONA, Antonino, ROSATELLI, Maria Cristina, PERRA, Chiara, FORTINA, Paolo, FERRARI, Maurizio

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Analysis of the GJB2 and GJB6 genes in Italian patients with nonsyndromic hearing loss: frequencies, novel mutations, genotypes, and degree of hearing loss von Primignani, Paola, Trotta, Luca, Castorina, Pierangela, Lalatta, Faustina, Sironi, Francesca, Radaelli, Chiara, Degiorgio, Dario, Curcio, Cristina, Travi, Maurizio, Ambrosetti, Umberto, Cesarani, Antonio, Garavelli, Livia, Formigoni, Patrizia, Milani, Donatella, Murri, Alessandra, Cuda, Domenico, Coviello, Domenico Antonio

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Identification of the new polymorphism IVS1-91 C→T in the beta globin gene von Primignani, Paola, Travi, Maurizio, Biasi, Anita, Sbrocca, Federica, Piga, Antonio, Scagni, Paola, Cantù Rajnoldi, Angelo

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Thalassaemia‐like carriers not linked to the β‐globin gene cluster von Faà, Valeria, Meloni, Alessandra, Moi, Loredana, Ibba, Giuseppe, Travi, Maurizio, Vitucci, Antonio, Cao, Antonio, Rosatelli, Maria Cristina

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Simultaneous mutations in the CLCNKB and SLC12A3 genes in two siblings with phenotypic heterogeneity in classic bartter syndrome von BETTINELLI, Alberto, BORSA, Nicolo, SYREN, Marie-Louise, MATTIELLO, Camilla, COVIELLO, Domenico, EDEFONTI, Alberto, GIANI, Marisa, TRAVI, Maurizio, TEDESCHI, Silvana

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GENETIC DIAGNOSIS BEFORE THE EIGHTH GESTATIONAL WEEK von Brambati, B, Tului, L., Travi, M.

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Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of {beta}-thalassemia von Galbiati, Silvia, Foglieni, Barbara, Travi, Maurizio, Curcio, Cristina, Restagno, Gabriella, Sbaiz, Luca, Smid, Maddalena, Pasi, Federica, Ferrari, Augusto, Ferrari, Maurizio, Cremonesi, Laura

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Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination von Percesepe, Antonio, Ferrari, Maurizio, Coviello, Domenico, Zanussi, Monica, Castagni, Marina, Neri, Isabella, Travi, Maurizio, Forabosco, Antonino, Tedeschi, Silvana

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A novel β-thalassemia mutation (G→A) at the initiation codon of the β-globin gene von Saba, L., Meloni, A., Sardu, R., Travi, M., Primignani, P., Rosatelli, M. C., Cao, A.

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Molecular characterization of hemoglobin C in sicily von Travi, M., Cremonesi, L., Primignani, P., di Benedetto, S., Testa, R., Schilirò, G., Ferrari, M.

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4 Molecular identification of complex alleles in the CFTR gene von Porcaro, L., Marchi, M., Capasso, P., Travi, M., Coviello, D., Degiorgio, D., Colombo, C., Romano, G., Claut, L., Padoan, R., Seia, M.

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Temperature-programmed capillary electrophoresis for the analysis of high-melting point mutants in thalassemias von Gelfi, Cecilia, Righetti, Pier Giorgio, Travi, Maurizio, Fattore, Silvia

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