Treated glass coverslips for in situ culture of amniotic cells: better cell adhesion and growth than on plastic.

nork Pecile, V, Archidiacono, N, Rocchi, M
Argitaratua 1984

Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis.

nork Rinaldi, A, Archidiacono, N, Rocchi, M, Filippi, G
Argitaratua 1979

Extra small metacentric chromosome identified as i(18p).

nork Rocchi, M, Stormi, M, Archidiacono, N, Filippi, G
Argitaratua 1979

Trisomy 20p from maternal t(3;20) translocation.

nork Archidiacono, N, Tecilazich, D, Tonini, G, Rocchi, M, Filippi, G
Argitaratua 1979

Centromere repositioning in mammals

nork Rocchi, M, Archidiacono, N, Schempp, W, Capozzi, O, Stanyon, R
Argitaratua 2012

(210)Po Log-normal distribution in human urines: Survey from Central Italy people

nork Sisti, D., Rocchi, M. B. L., Meli, M. A., Desideri, D.
Argitaratua 2009

X chromosome replication patterns in a case of X;9 balanced translocation.

nork Filippi, G, Pecile, V, Archidiacono, N, Baragino, E, Auber, G, Rocchi, M
Argitaratua 1983

A human alpha satellite DNA subset specific for chromosome 12.

nork Baldini, A, Rocchi, M, Archidiacono, N, Miller, O J, Miller, D A
Argitaratua 1990

A rapid and sensitive intracellular flow cytometric assay to identify Theileria parva infection within target cells

nork ROCCHI, M. S., BALLINGALL, K. T., NGUGI, D., MACHUGH, N. D., MCKEEVER, D. J.
Argitaratua 2007

Distal trisomy 6p and 20q owing to the concurrent transposition of distal 6p and 20q to the 22q telomere: a genomic polymorphism?

nork Bonaglia, M, Giorda, R, Cavallini, A, Pramparo, T, Rocchi, M, Borgatti, R, Zuffardi, O
Argitaratua 2003

Inversion polymorphisms and non‐contiguous terminal deletions: the cause and the (unpredicted) effect of our genome architecture

nork Ciccone, R, Mattina, T, Giorda, R, Bonaglia, M C, Rocchi, M, Pramparo, T, Zuffardi, O
Argitaratua 2006

Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effect.

nork Rocchi, M, Archidiacono, N, Rinaldi, A, Filippi, G, Bartolucci, G, Fancello, G S, Siniscalco, M
Argitaratua 1990

cDNA cloning, sequence analysis, and chromosomal localization of human carnitine palmitoyltransferase.

nork Finocchiaro, G, Taroni, F, Rocchi, M, Liras Martin, A, Colombo, I, Tarelli, G T, DiDonato, S
Argitaratua 1991

cDNA cloning, sequence analysis, and chromosomal localization of the gene for human carnitine palmitoyltransferase.

nork Finocchiaro, G, Taroni, F, Rocchi, M, Martin, A L, Colombo, I, Tarelli, G T, DiDonato, S
Argitaratua 1991

Isolation and characterization of the CRIPTO autosomal gene and its X-linked related sequence.

nork Dono, R, Montuori, N, Rocchi, M, De Ponti-Zilli, L, Ciccodicola, A, Persico, M G
Argitaratua 1991

A Fatal Case of Louping-ill in a Dog: Immunolocalization and Full Genome Sequencing of the Virus

nork Dagleish, M.P., Clark, J.J., Robson, C., Tucker, M., Orton, R.J., Rocchi, M.S.
Argitaratua izan da J Comp Pathol (2018)

The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.

nork Purrello, M, Alhadeff, B, Esposito, D, Szabo, P, Rocchi, M, Truett, M, Masiarz, F, Siniscalco, M
Argitaratua 1985

Leigh syndrome transmitted by uniparental disomy of chromosome 9

nork TIRANTI, V., LAMANTEA, E., UZIEL, G., ZEVIANI, M., GASPARINI, P., MARZELLA, R., ROCCHI, M., FRIED, M.
Argitaratua 1999

Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation.

nork Maestrini, E, Rivella, S, Tribioli, C, Rocchi, M, Camerino, G, Santachiara-Benerecetti, S, Parolini, O, Notarangelo, L D, Toniolo, D
Argitaratua 1992

Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis.

nork Ballabio, A, Parenti, G, Carrozzo, R, Sebastio, G, Andria, G, Buckle, V, Fraser, N, Craig, I, Rocchi, M, Romeo, G
Argitaratua 1987