Hall-Riggs syndrome: a possible second affected family?

Por SILENGO, M., RIGARDETTO, R.
Publicado em 2000

Ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosum: variable expression of a single syndrome?

Por Silengo, M, Silvestro, L, Capizzi, G, Lerone, M, Seri, M, Rosaia, L, Romeo, G
Publicado em 1998

Molecular characterisation of a supernumerary ring chromosome in a patient with VATER association

Por CINTI, R., PRIOLO, M., LERONE, M., GIMELLI, G., SERI, M., SILENGO, M., RAVAZZOLO, R.
Publicado em 2001

Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy.

Por Seri, M, Cusano, R, Forabosco, P, Cinti, R, Caroli, F, Picco, P, Bini, R, Morra, V B, De Michele, G, Lerone, M, Silengo, M, Pela, I, Borrone, C, Romeo, G, Devoto, M
Publicado em 1999

A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13

Por Morgan, N, Bacchelli, C, Gissen, P, Morton, J, Ferrero, G, Silengo, M, Labrune, P, Casteels, I, Hall, C, Cox, P, Kelly, D, Trembath, R, Scambler, P, Maher, E, Goodman, F, Johnson, C
Publicado em 2003

Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients

Por De Gregori, M, Ciccone, R, Magini, P, Pramparo, T, Gimelli, S, Messa, J, Novara, F, Vetro, A, Rossi, E, Maraschio, P, Bonaglia, M C, Anichini, C, Ferrero, G B, Silengo, M, Fazzi, E, Zatterale, A, Fischetto, R, Previderé, C, Belli, S, Turci, A, Calabrese, G, Bernardi, F, Meneghelli, E, Riegel, M, Rocchi, M, SGuerneri, Lalatta, F, Zelante, L, Romano, C, Fichera, Ma, Mattina, T, Arrigo, G, Zollino, M, Giglio, S, Lonardo, F, Bonfante, A, Ferlini, A, Cifuentes, F, Van Esch, H, Backx, L, Schinzel, A, Vermeesch, J R, Zuffardi, O
Publicado em 2007