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THREE CHROMOSOMES' (7; 9; 22) REARRANGEMENT AND THE ORIGIN OF THE PHILADELPHIA CHROMOSOMEFRANCESCONI D; PASQUALI F.1978; HUM. GENET.; DEU; DA. 1978; VOL. 43; NO 2; PP. 122-137; BIBL. 6 REF.Article

REARRANGEMENT OF THREE CHROMOSOMES (NOS 2, 8, AND 21) IN ACUTE MYELOBLASTIC LEUKEMIA. EVIDENCE FOR MORE THAN ONE SPECIFIC EVENTPASQUALI F; CASALONE R.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 3; NO 4; PP. 335-339; BIBL. 10 REF.Article

CHROMOSOME ABNORMALITIES AND MALE STERILITYZUFFARDI O; MARASCHIO P; PASQUALI F et al.1975; J. GENET. HUM.; SUISSE; DA. 1975; VOL. 23; NO 4; PP. 347-352; BIBL. 5 REF.Article

TRASLOCAZIONE CROMOSOMICA 6/17 CAUSA DI ABORTI RIPETUTI = TRANSLOCATION CHROMOSOMIQUE 6/17, CAUSE D'AVORTEMENTS REPETESPASQUALI F; MARASCHIO P; ZARA C et al.1973; ANN. OSTETR. GINECOL. MED. PERINAT.; ITAL.; DA. 1973; VOL. 94; NO 9-10; PP. 553-556; ABS. FR. ANGL.; BIBL. 4REF.Article

INVOLVEMENT OF CHROMOSOME NO.20 IN A COMPLEX PH1 TRANSLOCATION = ROLE DU CHROMOSOME NO 20 DANS LA TRANSLOCATION COMPLEXE DU PH1CASALONE R; BERNASCONI P; PASQUALI F et al.1983; CANCER GENETICS AND CYTOGENETICS; ISSN 0165-4608; NLD; DA. 1983; VOL. 8; NO 2; PP. 181-182; BIBL. 4 REF.; FIGArticle

THE ISOCHROMOSOME (179) IN CHRONIC MYELOCYTIC LEUKAEMIA: MECHANISM OF ORIGIN, CENTROMERIC FUNCTION AND CLONAL EVOLUTIONPASQUALI F; PANARELLO C; BERNASCONI P et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 1; PP. 89-90; BIBL. 11 REF.Article

A LIVERBORN TRIPLOID (69, XXY)FRANCESCONI D; MAGRINI U; PASQUALI F et al.1978; ANN. GENET.; FRA; DA. 1978; VOL. 21; NO 2; PP. 92-94; ABS. FRE; BIBL. 13 REF.Article

MASKED PHILADELPHIA CHROMOSOME CAUSED BY TRANSLOCATION (9; 11; 22) = CHROMOSOME DE PHILADELPHIE MASQUE CAUSE PAR LA TRANSLOCATION (9; 11; 22)SESSAREGO M; PASQUALI F; SCARRA GLB et al.1983; CANCER GENETICS AND CYTOGENETICS; ISSN 0165-4608; NLD; DA. 1983; VOL. 8; NO 4; PP. 319-323; ABS. ENG; BIBL. 11 REF.; FIGArticle

ISOCHROMOSOME (17Q) IN PHILADELPHIA CHROMOSOME (PH1)-NEGATIVE JUVENILE CHRONIC MYELOCYTIC LEUKEMIACASALONE R; FRANCESCONI D; PASQUALI F et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 3; NO 2; PP. 145-148; BIBL. 9 REF.Article

TRANSLOCATION T (2; 12) (P 25; Q21) CLASSEE D'ABORD COMME 2/XPASQUALI F; ZUFFARDI O; ZAMBONI G et al.1975; SEM. HOP., ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 1; PP. 64-66; ABS. ANGL.; BIBL. 12 REF.Article

PARTIAL TRISOMY 1 DUE TO 1/1 TRANSLOCATION IN PH'-POSITIVE CHRONIC MYELOCYTIC LEUKEMIAPASQUALI F; FRANCESCONI D; CASALONE R et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 3; PP. 277-282; BIBL. 16 REF.Article

WOMEN HETEROZYGOUS FOR DEFICIENCY OF THE (P21->PTER) REGION OF THE X CHROMOSOME ARE FERTILE.FRACCARO M; MARASCHIO P; PASQUALI F et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 3; PP. 283-291; BIBL. 16 REF.Article

COMMENT ON RUSSELL-SILVER SYNDROME = COMMENTAIRES SUR LE SYNDROME DE RUSSELL-SILVERSEVERI F; COLOMBO A; PASQUALI F et al.1974; PEDIATRICS; U.S.A.; DA. 1974; VOL. 54; NO 1; PP. 119; BIBL. 1REF.Article

Effects of carbohydrates on the ion conductance of the hemocxyanin channelMENESTRINA, G; PASQUALI, F.Zeitschrift fur Naturforschung. Section C, Biosciences. 1985, Vol 40, Num 1-2, pp 85-91, issn 0341-0382Article

THE 9P-DELETION SYNDROME. A PATIENT WITH A 45, XX, -9, -15, + T(9/15) CONSTITUTION DUE TO MATERNAL 3:1 MEIOTIC DISJUNCTION.BERGAMO F; CROSATO F; FRANCESCONI D et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 11; NO 3; PP. 219-223; BIBL. 10 REF.Article

TANDEM TRANSLOCATION 15/13PASQUALI F; ZUFFARDI O; SEVERI F et al.1973; SEM. HOP., ANN. GENET.; FR.; DA. 1973; VOL. 16; NO 1; PP. 47-50; ABS. FR.; BIBL. 11REF.Serial Issue

Full cytogenetic characterization of a new neuroblastoma cell line with a complex 17q translocationPANARELLO, C; MORERIO, C; RUSSO, I et al.Cancer genetics and cytogenetics. 2000, Vol 116, Num 2, pp 124-132, issn 0165-4608Article

Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemiaMASERATI, E; CAMPAGNOLI, E; TRUGLIO, F et al.Hereditas (Landskrona). 1989, Vol 111, Num 3, pp 305-308, issn 0018-0661Article

Cytogenetic pattern in leukemic cells of patients with constitutional chromosome anomaliesALIMENA, G; BILLSTROM, R; CASALONE, R et al.Cancer genetics and cytogenetics. 1985, Vol 16, Num 3, pp 207-218, issn 0165-4608Article

Ph-positive CML in blastic phase with monosomy 7 in a Down syndrome patient. Monitoring by interphase cytogenetics and demonstration of maternal allelic lossSEGHEZZI, L; DELLAVECCHIA, C; MASERATI, E et al.Cancer genetics and cytogenetics. 1997, Vol 99, Num 1, pp 77-80, issn 0165-4608Article

Translocation (8;21) in two cases of refractory anemia with excess of blasts in transformationMASERATI, E; CASALI, M; PASQUALI, F et al.Cancer genetics and cytogenetics. 1992, Vol 58, Num 1, pp 76-78, issn 0165-4608Article

Different break-points in Philadelphia chromosome variant translocations and in constitutional and sporadic translocationsMASERATI, E; PASQUALI, F; PERETTI, D et al.Annals of human genetics. 1986, Vol 50, Num 2, pp 153-162, issn 0003-4800Article

Point-mutated P21ras couples a muscarinic receptor to calcium channels and polyphosphoinositide hydrolysisCHIARUGI, V. P; PASQUALI, F; VANNUCCHI, S et al.Biochemical and biophysical research communications (Print). 1986, Vol 141, Num 2, pp 591-599, issn 0006-291XArticle

Phage types, ribotypes and tetracycline resistance genes of Salmonella enterica subsp. enterica serovar Typhimurium strains isolated from different origins in ItalyPASQUALI, F; DE CESARE, A; RICCI, A et al.Veterinary microbiology (Amsterdam). 2004, Vol 103, Num 1-2, pp 71-76, issn 0378-1135, 6 p.Article

Roberts syndrome : phenotypic variation, cytogenetic definition and heterozygote detectionMASERATI, E; PASQUALI, F; ZUFFARDI, O et al.Annales de génétique (Paris). 1991, Vol 34, Num 3-4, pp 239-246, issn 0003-3995Article

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