Barcoding Notch signaling in the developing brain von Siniscalco, Abigail M, Perera, Roshan Priyarangana, Greenslade, Jessie E, Veeravenkatasubramanian, Hemagowri, Masters, Aiden, Doll, Hannah M, Raj, Bushra

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Site-Specific Integration by Adeno-Associated Virus von Kotin, Robert M., Siniscalco, Marcello, Samulski, R. Jude, Zhu, Xiaodong, Hunter, Lynne, Laughlin, Catherine A., McLaughlin, Susan, Muzyczka, Nicholas, Rocchi, Marino, Berns, Kenneth I.

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Population genomics in Sardinia: a novel approach to hunt for genomic combinations underlying complex traits and diseases von Siniscalco, M., Robledo, R., Bender, P.K., Carcassi, C., Contu, L., Beck, J.C.

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The Role of Crk and Crkl Adaptor Proteins in the hair cells of Danio rerio inner ear and lateral line von Siniscalco, Abigail M

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Cytological Mapping of the Human Glucose-6-phosphate Dehydrogenase Gene Distal to the Fragile-X Site Suggests a High Rate of Meiotic Recombination across This Site von Szabo, Paul, Purrello, Michele, Rocchi, Mariano, Archidiacono, Nicoletta, Alhadeff, Becky, Filippi, Giorgio, Toniolo, Daniela, Martini, Giuseppe, Luzzatto, Lucio, Siniscalco, Marcello

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Chromosomes of Older Humans are More Prone to Aminopterine-Induced Breakage von Esposito, Diane, Fassina, Gianfranco, Szabo, Paul, De Angelis, Paula, Rodgers, Linda, Weksler, Marc, Siniscalco, Marcello

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A Human Autosomal Phosphoglycerate Kinase Locus Maps near the HLA Cluster von Szabo, Paul, Grzeschik, Karl-Heinz, Siniscalco, Marcello

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A 9.1-kb Gap in the Genome Reference Map Is Shown to Be a Stable Deletion/Insertion Polymorphism of Ancestral Origin von Robledo, Renato, Orru, Sandro, Sidoti, Antonella, Muresu, Rosella, Esposito, Diane, Grimaldi, Marie Claude, Carcassi, Carlo, Rinaldi, Antoniettina, Bernini, Luigi, Contu, Licinio, Romani, Massimo, Roe, Bruce, Siniscalco, Marcello

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Giorgio Filippi, April 4, 1935-January 19, 1996 von Siniscalco, Marcello

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Human genome mapping and its medical perspectives von Siniscalco, M

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The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3 von Purrello, M., Alhadeff, B., Esposito, D., Szabo, P., Rocchi, M., Truett, M., Masiarz, F., Siniscalco, M.

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In situ mapping of the gene coding for a leucine zipper DNA binding protein (CDR62) to 16p12–16p13.1 von Gress, T., Baldini, A., Rocchi, M., Furneaux, H., Posner, J.B., Siniscalco, M.

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A Novel Approach to Search for Identity by Descent in Small Samples of Patients and Controls from the Same Mendelian Breeding Unit: A Pilot Study on Myopia von Heath, Simon, Robledo, Renato, Beggs, William, Feola, Gaetano, Parodo, Carlo, Rinaldi, Antoniettina, Contu, Licinio, Dana, Debra, Stambolian, Dwight, Siniscalco, Marcello

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A plea to search for deletion polymorphism through genome scans in populations von Siniscalco, Marcello, Robledo, Renato, Orru, Sandro, Contu, Licinio, Yadav, Prem, Ren, Qun, Lai, Hongshing, Roe, Bruce

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The myoblast defect identified in Duchenne muscular dystrophy is not a primary expression of the DMD mutation: clonal analysis of myoblasts from five double heterozygotes for two X... von WEBSTER, C, FILIPPI, G, RINALDI, A, MASTROPAOLO, C, TONDI, M, SINISCALCO, M, BLAU, H. M

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An anonymous single copy X-chromosome clone DXS92, from Xq26–27, identifies two frequent RFLPs von Davatelis, G., Siniscalco, M., Szabo, P.

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An anonymous single copy X-chromosome clone DXS91, from Xq11-q13, identifies a moderately frequent RFLP von Davatelis, G., Siniscalco, M., Szabo, P.

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Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia von Rinaldi, A, Filippi, G, Siniscalco, M

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X-linkage of steroid sulphatase in the mouse is evidence for a functional Y-linked allele von Keitges, E, Rivest, M, Siniscalco, M, Gartler, S. M

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Changes in Toadfish Acoustic Behavior in Relation to Tourism in Panama von Siniscalco, Abigail M, Dean, Emily E, May-Collado, Laura J

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