Sfoglia per Autore
Chromosome 14 maternal uniparental disomy in the euploid cell line of a fetus with mosaic 46,XX/47,XX,+14 karyotype
1994 S.M. Sirchia, C. De Andreis, S. Pariani, M.G. Grimoldi, A. Molinari, M. Buscaglia, G. Simoni
Confined placental mosaicism
1994 G. Simoni, S.M. Sirchia
Severe epilepsy in a patient with Prader-Willi-syndrome due to inversion-duplication of chromosome 15q11-q13 - a clinical neurophysiological, and molecular-genetic study
1995 U. Aguglia, A. Gambardella, D. Concolino, G. Porta, S. Sirchia, A. Quattrone
Molecular screening of families affected by familial adenomatous polyposis (FAP)
1996 I. Gazzoli, C. De Andreis, S.M. Sirchia, P. Sala, C. Rossetti, L. Bertario, G. Colucci
Aneuploid correction and confined placental mosaicism
1996 G. Simoni, S.M. Sirchia, M. Fraccaro
Characterization of four microsatellites in an Italian population and their application to paternity testing
1996 S.M. Sirchia, I. Garagiola, C. De Andreis, I. Gazzoli, M. Gramegna, G. Colucci
Cytogenetic abnormalities and microsatellite instability in endometrial adenocarcinoma
1997 S.M. Sirchia, S. Pariani, F. Rossella, I. Garagiola, C. De Andreis, G. Bulfamante, E. Zannoni, U. Radaelli, G. Simoni
Highly sensitive chemiluminescent method for the detection of maternal cell contamination in human cord blood stored for allotransplantation : the experience of the Milano cord blood bank
1997 F. Poli, L. Crespiatico, L. Lecchi, G. Sirchia, M. Scalamogna, S.M. Sirchia, I. Garagiola, L. Pedranzini
Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected
1997 C. De Andreis, G. Simoni, C. Castagna, L. Sacchi, S.M. Sirchia, I.M. Garagiola, T. Persico, P. Serafini, G. Pardi, A.E. Semprini
Detection of maternal DNA in human cord blood stored for allotransplantation by a highly sensitive chemiluminescent method
1997 F. Poli, S.M. Sirchia, M. Scalamogna, I. Garagiola, L. Crespiatico, L. Pedranzini, L. Lecchi, G. Sirchia
Intrauterine growth retardation (IUGR) : uniparental disomy or placental morpho-functional anomalies?
1998 R. Malgara, M.G. Grimoldi, E. Meroni, A. Benevento, G. Bulfamante, S.M. Sirchia
Trisomic zygote rescue revealed by DNA polymorphism analysis in confined placental mosaicism
1998 S.M. Sirchia, I. Garagiola, G. Colucci, S. Guerneri, F. Lalatta, M.G. Grimoldi, G. Simoni
Highly sensitive chemiluminescent method for the detection of cell contamination
1998 S.M. Sirchia, I. Garagiola, C. De Andreis, L. Pedranzini, F. Poli, F.R. Grati, B. Diomelli, G. Simoni
Emotion-induced myoclonic absence-like seizures in a patient with inv-dup(15) syndrome : a clinical, EEG, and molecular genetic study
1999 U. Aguglia, E. Le Piane, A. Gambardella, D. Messina, C. Russo, S.M. Sirchia, G. Porta, A. Quattrone
Silencing of the retinoic acid receptor beta (RAR beta) gene by hypermethylation in human breast cancer
1999 S. Sirchia, A.T. Ferguson, S. Sukumar, R. Orlandi, N. Sacchi
Loss of heterozigosity of chromosomal region 4q32-35 in basal cell carcinomas
2000 E. Sironi, S. Sirchia, A. Cerri, F. Rossella, F. Grati, R. Calcaterra, D. Tomasini, G. Simoni
Evidence of epigenetic changes affecting the chromatin state of the retinoic acid receptor beta2 promoter in breast cancer cells
2000 S.M. Sirchia, A.T. Ferguson, E. Sironi, S. Subramanyan, R. Orlandi, S. Sukumar, N. Sacchi
Detection of maternal DNA in cord blood at birth after elective caesarean section or vaginal delivery
2000 A.E. Semprini, C. De Andreis, S. Fiore, I. Garagiola, S.M. Sirchia, V. Savasi, M.L. Newell, G. Simoni
Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas
2000 F.R. Grati, S.M. Sirchia, I. Garagiola, E. Sironi, S. Galioto, F. Rossella, P. Serafini, F. Dulcetti, A. Bozzetti, R. Brusati, G. Simoni
Losses of heterozygosity in endometrial adenocarcinomas : positive correlations with histopathological parameters
2000 S.M. Sirchia, E. Sironi, F.R. Grati, P. Serafini, I. Garagiola, F. Rossella, F. Dulcetti, G. Pardi, S. Garsia, G. Simoni
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