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Results: 1-25 | 26-50
Results: 1-25/50
IN-VIVO DIFFERENTIATION OF MAST-CELLS FROM ACUTE MYELOID-LEUKEMIA BLASTS CARRYING A NOVEL ACTIVATING LIGAND-INDEPENDENT C-KIT MUTATION
Authors: BEGHINI A CAIROLI R MORRA E LARIZZA L
Citation: A. Beghini et al., IN-VIVO DIFFERENTIATION OF MAST-CELLS FROM ACUTE MYELOID-LEUKEMIA BLASTS CARRYING A NOVEL ACTIVATING LIGAND-INDEPENDENT C-KIT MUTATION, Blood cells, molecules, & diseases (Print), 24(12), 1998, pp. 262-270
CHOANAL ATRESIA AS SOLE CONSEQUENCE OF THE 45,XX,DER(9)T(9-22)(P24-Q12)MAT,-22 KARYOTYPE
Authors: BETTIO D GOTTARDI G RIZZI N GIARDINO D INTROVINI P LARIZZA L
Citation: D. Bettio et al., CHOANAL ATRESIA AS SOLE CONSEQUENCE OF THE 45,XX,DER(9)T(9-22)(P24-Q12)MAT,-22 KARYOTYPE, European journal of human genetics, 6, 1998, pp. 2006-2006
FISH CHARACTERIZATION OF 2 SUPERNUMERARY R(1) ASSOCIATED WITH CLINICAL PHENOTYPE
Authors: GIARDINO D BETTIO D GOTTARDI G RIZZI N PIERLUIGI M PERFUMO C CALI A BRICARELLI FD LARIZZA L
Citation: D. Giardino et al., FISH CHARACTERIZATION OF 2 SUPERNUMERARY R(1) ASSOCIATED WITH CLINICAL PHENOTYPE, European journal of human genetics, 6, 1998, pp. 2007-2007
HIGH-LEVEL TRISOMY-8 MOSAICISM IN PERIPHERAL-BLOOD LYMPHOCYTES FROM AROTHMUND-THOMSON-SYNDROME PATIENT
Authors: CASTORINA P MIOZZO M MODIANO P FURHMANCONTI AM CROQUETTE MF LARIZZA L
Citation: P. Castorina et al., HIGH-LEVEL TRISOMY-8 MOSAICISM IN PERIPHERAL-BLOOD LYMPHOCYTES FROM AROTHMUND-THOMSON-SYNDROME PATIENT, European journal of human genetics, 6, 1998, pp. 2062-2062
IDENTIFICATION OF THE ORIGIN OF A RARE CHROMOSOME 5Q HETEROCHROMATIC VARIANT BY FISH
Authors: LUISA D GANDOLFI P NOCERA G LARIZZA L
Citation: D. Luisa et al., IDENTIFICATION OF THE ORIGIN OF A RARE CHROMOSOME 5Q HETEROCHROMATIC VARIANT BY FISH, European journal of human genetics, 6, 1998, pp. 2070-2070
NON SPECIFIC X-LINKED MENTAL-RETARDATION IN A SARDINIAN FAMILY
Authors: RUSSO S COGLIATI F MACCHI M LARIZZA L
Citation: S. Russo et al., NON SPECIFIC X-LINKED MENTAL-RETARDATION IN A SARDINIAN FAMILY, European journal of human genetics, 6, 1998, pp. 4148-4148
UNIPARENTAL DISOMY AND PEG1 MEST GENE IN SILVER-RUSSELL-SYNDROME/
Authors: COGLIATI F RUSSO S MACCHI M SELICORNI A BEDESCHI MF NATACCI F PARINI R LARIZZA L
Citation: F. Cogliati et al., UNIPARENTAL DISOMY AND PEG1 MEST GENE IN SILVER-RUSSELL-SYNDROME/, European journal of human genetics, 6, 1998, pp. 4217-4217
TRISOMY 4 AND C-KIT MUTATION IN A T(8-21) MYELOID-LEUKEMIA WITH MAST-CELL INVOLVEMENT
Authors: BEGHINI A CASTORINA P CAIROLI R RIPAMONTI C MORRA E LARIZZA L
Citation: A. Beghini et al., TRISOMY 4 AND C-KIT MUTATION IN A T(8-21) MYELOID-LEUKEMIA WITH MAST-CELL INVOLVEMENT, Cytogenetics and cell genetics, 81(2), 1998, pp. 160-160
19P13.12-PTER DELETION IN MULTIPLE LEIOMYOSARCOMAS FROM THE SAME PATIENT
Authors: RIVA P MALGARA R DALPRA L VOLONTE M GUALANDRI V CONTI AMF LARIZZA L
Citation: P. Riva et al., 19P13.12-PTER DELETION IN MULTIPLE LEIOMYOSARCOMAS FROM THE SAME PATIENT, Cytogenetics and cell genetics, 81(2), 1998, pp. 192-192
TRANSLOCATION (7-17)(Q22-P13) AS A SOLE KARYOTYPIC CHANGE IN AN ADRENAL ADENOMA
Authors: BETTIO D RIZZI N GIARDINO D VIRDUCI T LOLI P LARIZZA L
Citation: D. Bettio et al., TRANSLOCATION (7-17)(Q22-P13) AS A SOLE KARYOTYPIC CHANGE IN AN ADRENAL ADENOMA, Cancer genetics and cytogenetics, 103(2), 1998, pp. 180-181
MOLECULAR CHARACTERIZATION OF FRAXE-POSITIVE SUBJECTS WITH MENTAL IMPAIRMENT IN 2 UNRELATED ITALIAN FAMILIES
Authors: RUSSO S SELICORNI A BEDESCHI MF NATACCI F VIZIELLO P FORTUNA R PAGANI G DALPRA L LARIZZA L
Citation: S. Russo et al., MOLECULAR CHARACTERIZATION OF FRAXE-POSITIVE SUBJECTS WITH MENTAL IMPAIRMENT IN 2 UNRELATED ITALIAN FAMILIES, American journal of medical genetics, 75(3), 1998, pp. 304-308
CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM 2 SIBS WITH ROTHMUND-THOMSON-SYNDROME
Authors: MIOZZO M CASTORINA P RIVA P DALPRA L CONTI AMF VOLPI L HOE TS KHOO A WIEGANT J ROSENBERG C LARIZZA L
Citation: M. Miozzo et al., CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM 2 SIBS WITH ROTHMUND-THOMSON-SYNDROME, International journal of cancer, 77(4), 1998, pp. 504-510
AN UNUSUAL FRAGILE-X SIBSHIP - FEMALE COMPOUND HETEROZYGOTE AND MALE WITH A PARTIALLY METHYLATED FULL MUTATION
Authors: RUSSO S BRISCIOLI V COGLIATI F MACCHI M LALATTA F LARIZZA L
Citation: S. Russo et al., AN UNUSUAL FRAGILE-X SIBSHIP - FEMALE COMPOUND HETEROZYGOTE AND MALE WITH A PARTIALLY METHYLATED FULL MUTATION, Clinical genetics, 54(4), 1998, pp. 309-314
IN-VIVO DIFFERENTIATION OF MAST-CELLS FROM AML M2 BLASTS CARRYING A NOVEL ACTIVATING LIGAND-INDEPENDENT C-KIT MUTATION
Authors: BEGHINI A CAIROLI R MORRA E LARIZZA L
Citation: A. Beghini et al., IN-VIVO DIFFERENTIATION OF MAST-CELLS FROM AML M2 BLASTS CARRYING A NOVEL ACTIVATING LIGAND-INDEPENDENT C-KIT MUTATION, British Journal of Haematology, 102(1), 1998, pp. 13-13
C-KIT ACTIVATING MUTATIONS AND MAST-CELL PROLIFERATION IN HUMAN LEUKEMIA
Authors: BEGHINI A LARIZZA L CAIROLI R MORRA E
Citation: A. Beghini et al., C-KIT ACTIVATING MUTATIONS AND MAST-CELL PROLIFERATION IN HUMAN LEUKEMIA, Blood, 92(2), 1998, pp. 701-702
11 X-CHROMOSOME BREAKPOINTS ASSOCIATED WITH PREMATURE OVARIAN FAILURE(POF) MAP TO A 15-MB YAC CONTIG SPANNING XQ21
Authors: SALA C ARRIGO G TORRI G MARTINAZZI F RIVA P LARIZZA L PHILIPPE C JONVEAUX P SLOAN F LABELLA T TONIOLO D
Citation: C. Sala et al., 11 X-CHROMOSOME BREAKPOINTS ASSOCIATED WITH PREMATURE OVARIAN FAILURE(POF) MAP TO A 15-MB YAC CONTIG SPANNING XQ21, Genomics, 40(1), 1997, pp. 123-131
PAST AND FUTURE CYTOGENETIC TOOLS TO IDENTIFY GENES INVOLVED IN DEVELOPMENT AND PROGRESSION OF SOLID TUMORS
Authors: LARIZZA L
Citation: L. Larizza, PAST AND FUTURE CYTOGENETIC TOOLS TO IDENTIFY GENES INVOLVED IN DEVELOPMENT AND PROGRESSION OF SOLID TUMORS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 94-94
HIGH CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM A SIBSHIP OF AN INBRED PEDIGREE WITH ROTHMUND-THOMSON SYNDROME (RTS)
Authors: CASTORINA P MIOZZO M RIVA P CONTI AMF WIEGANT J ROSENBERG C DALPRA L VOLPI L MAK JW LARIZZA L
Citation: P. Castorina et al., HIGH CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM A SIBSHIP OF AN INBRED PEDIGREE WITH ROTHMUND-THOMSON SYNDROME (RTS), Cytogenetics and cell genetics, 77(1-2), 1997, pp. 103-103
EXPRESSION OF RARE FRA10Q24 - CHROMOSOME TRUNCATION, AMPLIFICATION OFDISTAL SEGMENT AND TELOMERE RENEWAL
Authors: VILLA N DALPRA L LARIZZA L
Citation: N. Villa et al., EXPRESSION OF RARE FRA10Q24 - CHROMOSOME TRUNCATION, AMPLIFICATION OFDISTAL SEGMENT AND TELOMERE RENEWAL, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 293-293
CYTOGENETIC STUDY OF PITUITARY-ADENOMA
Authors: BETTIO D RIZZI N GIARDINO D PERSANI L PECORIGIRALDI F LOSA M LARIZZA L
Citation: D. Bettio et al., CYTOGENETIC STUDY OF PITUITARY-ADENOMA, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 356-356
CYTOGENETIC CHARACTERIZATION OF A CLIVUS CHORDOMA IN A CANCER FAMILY PATIENT
Authors: MIOZZO M MALGARA R RIVA P VOLONTE M LARIZZA L CONTI AMF DALPRA L
Citation: M. Miozzo et al., CYTOGENETIC CHARACTERIZATION OF A CLIVUS CHORDOMA IN A CANCER FAMILY PATIENT, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 369-369
CYTOGENETIC FINDINGS ON MULTIPLE LEIOMYOSARCOMA THE SAME PATIENT
Authors: RIVA P MALGARA R DALPRA L VOLONTE M GUALANDRI V CONTI AMF LARIZZA L
Citation: P. Riva et al., CYTOGENETIC FINDINGS ON MULTIPLE LEIOMYOSARCOMA THE SAME PATIENT, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 378-378
CYTOGENETIC STUDY OF PITUITARY-ADENOMAS
Authors: BETTIO D RIZZI N GIARDINO D PERSANI L PECORIGIRALDI F LOSA M LARIZZA L
Citation: D. Bettio et al., CYTOGENETIC STUDY OF PITUITARY-ADENOMAS, Cancer genetics and cytogenetics, 98(2), 1997, pp. 131-136
GENOTYPE-PHENOTYPE CORRELATION IN 2 SETS OF MONOZYGOTIC TWINS WITH WILLIAMS-SYNDROME
Authors: CASTORINA P SELICORNI A BEDESCHI F DALPRA L LARIZZA L
Citation: P. Castorina et al., GENOTYPE-PHENOTYPE CORRELATION IN 2 SETS OF MONOZYGOTIC TWINS WITH WILLIAMS-SYNDROME, American journal of medical genetics, 69(1), 1997, pp. 107-111
EXPRESSION OF 3 RARE FRAGILE SITES - CHROMOSOMAL TRUNCATION, AMPLIFICATION OF DISTAL SEGMENT AND TELOMERIC RENEWAL
Authors: VILLA N DALPRA L LARIZZA L
Citation: N. Villa et al., EXPRESSION OF 3 RARE FRAGILE SITES - CHROMOSOMAL TRUNCATION, AMPLIFICATION OF DISTAL SEGMENT AND TELOMERIC RENEWAL, Chromosoma, 106(6), 1997, pp. 400-404
Risultati: 1-25 | 26-50