Sfoglia per Autore
The CFC syndrome--report of the first two cases outside the United States.
1987 G. Neri;G. Sabatino;E. Bertini;M. Genuardi
A girl with G syndrome and agenesis of the corpus callosum.
1987 G. Neri;M. Genuardi;G. Natoli;P. Costa;G. Maggioni
Partial duplication of chromosome 1q preceding the development of an L3 lymphoblastic leukemia with t(8;14), secondary to treatment for Hodgkin's disease.
1988 M. Zollino;M. Genuardi;R. D. Santis;G. Leone;R. Marra;R. Mancini;G. Mango;G. Neri
Localization of the HLA class II-associated invariant chain gene to human chromosome band 5q32.
1988 M. Genuardi;G. F. Saunders
Long-term cytogenetic effects of antineoplastic treatment in relation to secondary leukemia.
1988 M. Genuardi;M. Zollino;A. Serra;G. Leone;R. Mancini;G. Mango;G. Neri
Partial tetrasomy 9 in an infant with clinical and radiological evidence of multiple joint dislocations.
1988 F. Calvieri;C. Tozzi;C. Benincori;M. V. De;A. Bellussi;M. Genuardi;G. Neri
Distal deletion of chromosome Ip in ductal carcinoma of the breast.
1989 M. Genuardi;H. Tsihira;D. E. Anderson;G. F. Saunders
Brachy/ectrodactyly and absence or hypoplasia of the fibula: an autosomal dominant condition with low penetrance and variable expressivity.
1990 M. Genuardi;M. Zollino;A. Bellussi;W. Fuhrmann;G. Neri
Analysis of 138 consecutive ovarian cancer patients: incidence and characteristics of familial cases.
1990 S. Greggi;M. Genuardi;P. Benedetti-Panici;R. Cento;G. Scambia;G. Neri;S. Mancuso
Differential expression of FRA16B in peripheral lymphocytes and bone marrow cells.
1990 M. Zollino;M. Genuardi;G. Neri
Genomic changes on the short arm of human chromosome 1 in breast cancer.
1991 W. M. Mars;M. Genuardi;H. Tsihira;D. E. Anderson;G. F. Saunders
Chronic myelogenous leukemia in the course of chronic lymphocytic leukemia: evidence for an independent clonal origin.
1991 M. Zollino;M. Genuardi;P. Tanci;G. Mango;C. Rumi;R. Mancini;G. Neri
Effects of dexamethasone on the growth and epidermal growth factor receptor expression of the OVCA 433 ovarian cancer cells.
1992 G. Ferrandina;G. Scambia;P. B. Panici;G. Bonanno;R. D. Vincenzo;C. Rumi;S. Bussa;M. Genuardi;V. R. Spica;V. S. Romano;S. Mancuso
Dosage analysis at the CSF1 and CSF1R loci in a new case of partial trisomy 5q.
1992 M. Genuardi;R. Flamia;G. Palka;G. Parruti;G. Neri
PCR detection of an insertion/deletion polymorphism in intron 1 of the HRAS1 locus.
1992 P. Tanci;M. Genuardi;S. A. Santini;G. Neri
Creutzfeldt-Jakob disease after non-commercial dura mater graft
1992 M. Pocchiari;C. Masullo;M. Salvatore;M. Genuardi;S. Galgani
X-linked VACTERL with hydrocephalus: the VACTERL-H syndrome.
1993 M. Genuardi;P. Chiurazzi;A. Capelli;G. Neri
Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3.
1993 L. Kozák;P. Chiurazzi;M. Genuardi;M. G. Pomponi;M. Zollino;G. Neri
A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.
1993 M. Pocchiari;M. Salvatore;F. Cutruzzolá;M. Genuardi;C. T. Allocatelli;C. Masullo;G. Macchi;G. Alemá;S. Galgani;Y. G. Xi
Split hand/split foot anomaly in a family segregating a balanced translocation with breakpoint on 7q22.1.
1993 M. Genuardi;M. G. Pomponi;V. Sammito;A. Bellussi;M. Zollino;G. Neri
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