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CANCER GENETICS AND CYTOGENETICS
Rivista
Codice:
E032026
ISSN:
0165-4608
Dati Generali
Dati Generali
Pubblicazioni (41)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
A clonal t(),12)(q32q21) in cultured fibroblasts from a case of Bowen's disease.
Articolo
A complex translocation (5;7) in a patient with acute nonlymphocytic leukemia evolved from a myelodysplastic syndrome.
Articolo
A search for double minute chromosomes in cultured lymphocytes from different types of tumors.
Articolo
ABL1 amplification in T-cell acute lymphoblastic leukemia.
Articolo
Amplification of the pericentromeric region of chromosome 1 in a newly established colon carcinoma cell line
Articolo
Chromosome abnormalities in a case of pituitary adenoma.
Articolo
Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1.
Articolo
Chromosome instability in cultured lymphocytes of patients with ovarian or uterine cancer.
Articolo
Clonal chromosome abnormalities with preferential ilvolvement of chromosome 3 in patient with Porokeratosi of Mibelli.
Articolo
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.
Articolo
Cytogenetic findings in a case of anaplastic carcinoma of the pancreas.
Articolo
Cytogenetic of multiple endocrine neoplasia syndromes. I. Two different, unique clonal chromosome changes in a medullary thyroid carcinoma and in a C-cell thyroid hyperplasia.
Articolo
Cytogenetic studies in venous tissues from patients with vericose venis.
Articolo
Cytogenetics of multiple endocrine neoplasia syndrome. II. Chromosome abnormalities in an insulinoma and a Glaucoma from two subjects with MEN1.
Articolo
DNA amplification in human gastric carcinomas
Articolo
Detection of TET2 abnormalities by fluorescence in situ hybridization in 41 patients with myelodysplastic syndromes
Articolo
Different genome organization in two new cell lines established from human gastric carcinoma.
Articolo
Duplication of the der(14) chromosome of a translocation (8;14) in a case of Burkitt's type L3-ALL.
Articolo
Early onset of gastric carcinoma and constitutional deletion of 18p.
Articolo
FAMILIAL PARTIAL MONOSOMY 7 AND MYELODYSPLASIA: DIFFERENT PARENTAL ORIGIN OF THE 7 INVOLVED SUGGESTS THE ACTION OF A MUTATOR GENE
Articolo
Familial myelodysplastic syndromed, monosomy 7/trisomy 8, and mutator effects.
Articolo
Familial partial monosomy 7 and myelodysplasia : different parental origin of the monosomy 7 suggests action of a mutator gene
Articolo
Graft-versus-leukemia effects after allogeneic bone marrow transplantation are active also in the presence of clones with chromosomal anomalies in addition to the Ph chromosome.
Articolo
Involvement of chromosome n20 in a complex Ph1 translocation
Articolo
Isochromosome (7) (q10) in Schwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders.
Articolo
Isochromosome (7)(q10) in Shwachman Syndrome Without MDS/AML and Role of Chromosome 7 Anomalies in Myeloproliferative Disorders
Articolo
Isochromosome 7q10 in Shwachman Syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders.
Articolo
Jumping translocations in acute lymphoblastic leukemia.
Articolo
Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas.
Articolo
Malignant melanoma: sister chromatid exchange analysis in three families.
Articolo
Multiple clonal chromosome abnormalities in a superficial basal cell epithelioma.
Articolo
Parental origin of chromosomes 9 and 22 involved in the Ph chromosome translocation in chronic myelocytic leukemia.
Articolo
Ph- positive CML in blastic phase with monosomy 7 in a Down syndrome patient. Monitoring by interphase cytogenetics and demonstration of maternal allelic loss.
Articolo
Ph-positive CML in blastic phase with monosomy 7 in a Down syndrome patient. Monitoring by interphase cytogenetics and demonstration of maternal allelic loss.
Articolo
Sister chromatid exchange and proliferation pattern in stimulated lymphocytes of cutaneous malignant melanoma patients.
Articolo
Study on aneuploidy and p53 mutations in astrocytomas
Articolo
Telomeric fusions in cultured human fibroblasts as a source of genomic instability.
Articolo
Translocation (8;21) in two cases of refractory anaemia with excess of blasts in transformation
Articolo
Translocation (8;21) in two cases of refractory anemia with excess of blasts in transformation.
Articolo
Trisomy 11 and a complex t(11;11;22) in a patient with acute myelomonocytic leukemia (AML-M4) following myelodysplasia (MDS): a cytogenetic study of a mechanism of leukemogenesis.
Articolo
Trisomy 12 in a case of large cell, immunoblastic, polymorphous non-Hodgkin’s lymphoma with Ig Gk monoclonal paraprotein
Articolo
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