检索结果 - P Maraschio
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Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation 由 Elena Rossi, Mariluce Riegel, Jole Messa, Stefania Gimelli, P Maraschio, Roberto Ciccone, Michela Stroppi, Paola Riva, Concetta Simona Perrotta, Teresa Mattina, L. Memo, Alessandra Baumer, Vaidutis Kučinskas, Claudio Castellan, Albert Schinzel, Orsetta Zuffardi
出版 2007Artigo -
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13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients 由 Lucia Ballarati, Elena Rossi, Maria Teresa Bonati, Stefania Gimelli, P Maraschio, Palma Finelli, Sabrina Giglio, Elisabetta Lapi, Maria Francesca Bedeschi, Silvana Guerneri, Giulia Arrigo, Maria Grazia Patricelli, Teresa Mattina, O. Guzzardi, Vanna Pecile, Adalgisa Police, Gioacchino Scarano, Lidia Larizza, Orsetta Zuffardi, Daniela Giardino
出版 2006Carta -
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Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients 由 Manuela De Gregori, Roberto Ciccone, Pamela Magini, Tiziano Pramparo, Stefania Gimelli, Jole Messa, Francesca Novara, Annalisa Vetro, Elena Rossi, P Maraschio, María Clara Bonaglia, Cecilia Anichini, Giovanni Battista Ferrero, Margherita Silengo, Elisa Fazzi, Adriana Zatterale, Rita Fischetto, Carlo Previderé, S. Belli, Alessandra Turci, G Calabrese, Franca Bernardi, Emanuela Meneghelli, Mariluce Riegel, Mariano Rocchi, Silvana Guerneri, Faustina Lalatta, Leopoldo Zelante, Corrado Romano, Marco Fichera, Teresa Mattina, Giulia Arrigo, Marcella Zollino, Sabrina Giglio, Fortunato Lonardo, Aldo Bonfante, Alessandra Ferlini, Francisco Tejada Cifuentes, Hilde Van Esch, Liesbeth Backx, Albert Schinzel, Joris Vermeesch, Orsetta Zuffardi
出版 2007Artigo
相关主题
Biology
Chromosome
Gene
Genetics
Phenotype
Karyotype
Chromosomal rearrangement
Comparative genomic hybridization
Breakpoint
Chromosomal translocation
Chromosome 13
Cytogenetics
DNA
DNA damage
Facioscapulohumeral muscular dystrophy
Fluorescence in situ hybridization
Gene duplication
Genetic linkage
Genome instability
Haploinsufficiency
Locus (genetics)
Monosomy
Muscular dystrophy
Position effect
Ring chromosome
Subtelomere
Telomere
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