AAAAAA

   
Results: 1-12 |
Results: 12

Authors: CAVANI S PERFUMO C ARGUSTI A PIERLUIGI M PERRONI L SCMIEGELOW K PETERSEN MB COTTER FE STRIGINI P DAGNABRICARELLI F NIZETIC D
Citation: S. Cavani et al., CYTOGENETIC AND MOLECULAR STUDY OF 32 DOWN-SYNDROME FAMILIES - POTENTIAL LEUKEMIA PREDISPOSING ROLE OF THE MOST PROXIMAL SEGMENT OF CHROMOSOME-21Q, British Journal of Haematology, 103(1), 1998, pp. 213-216

Authors: LOPINTO G GALLETTI A ARGUSTI A BARONE E VASSALLO S ROMANO L PERRONI L
Citation: G. Lopinto et al., APC RESISTANCE AND CYSTIC-FIBROSIS IN THE SAME FAMILY, Thrombosis and haemostasis, 1997, pp. 1292-1292

Authors: BRICARELLI FD ARGUSTI A CAVANI S FORABOSCO A
Citation: Fd. Bricarelli et al., CYTOGENETIC ANALYSIS GUIDELINES AND LABORATORIES ORGANIZATION IN ITALY, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 69-69

Authors: CAVANI S PIERLUIGI M PERFUMO C ARGUSTI A PERRONI L STRIGINI P BRICARELLI FD
Citation: S. Cavani et al., HIGH-FREQUENCY OF PATERNAL CHROMOSOME-21 NONDISJUNCTION IN ITALIAN FAMILIES, Cytogenetics and cell genetics, 77, 1997, pp. 9-9

Authors: DAGNABRICARELLI F ARGUSTI A CAVANI S PIERLUIGI M PERFUMO C PERRONI L STRIGINI P COTTER P NIZETIC D
Citation: F. Dagnabricarelli et al., MOLECULAR STUDY OF 17 DS-FAMILIES WITH LEUKEMIA USING POLYMORPHIC MARKERS FROM CHROMOSOME-21, Cytogenetics and cell genetics, 77, 1997, pp. 31-31

Authors: SEGHEZZI L DELLAVECCHIA C MASERATI E MINELLI A CARRA A LOCATELLI F ARGUSTI A LOCURTO F DANESINO C PASQUALI F
Citation: L. Seghezzi et al., PH-POSITIVE CML IN BLASTIC PHASE WITH MONOSOMY-7 IN A DOWN-SYNDROME PATIENT - MONITORING BY INTERPHASE CYTOGENETICS AND DEMONSTRATION OF MATERNAL ALLELIC LOSS, Cancer genetics and cytogenetics, 99(1), 1997, pp. 77-80

Authors: PERRONI L GRASSO M GARAVELLI L ARGUSTI A CAVANI S LONIGRO C BRICARELLI FD
Citation: L. Perroni et al., 3 CASES OF HIGH-FUNCTIONING FRAGILE-X MALES, American journal of human genetics, 61(4), 1997, pp. 614-614

Authors: PERRONI L GRASSO M ARGUSTI A NIGRO CL CROCI GF ZELANTE L GARANI GP BRICARELLI FD
Citation: L. Perroni et al., MOLECULAR AND CYTOGENETIC ANALYSIS OF THE FRAGILE-X SYNDROME IN A SERIES OF 453 MENTALLY-RETARDED SUBJECTS - A STUDY OF 87 FAMILIES (VOL 64, PG 176, 1996), American journal of medical genetics, 66(1), 1996, pp. 118-118

Authors: PERRONI L GRASSO M ARGUSTI A LONIGRO C CROCI GF ZELANTE L GARANI GP BRICARELLI FD
Citation: L. Perroni et al., MOLECULAR AND CYTOGENETIC ANALYSIS OF THE FRAGILE-X-SYNDROME IN A SERIES OF 453 MENTALLY-RETARDED SUBJECTS - A STUDY OF 87 FAMILIES, American journal of medical genetics, 64(1), 1996, pp. 176-180

Authors: GRASSO M PERRONI L COLELLA S PIOMBO G ARGUSTI A LITUANIA M BUSCAGLIA M GIUSSANI U GRIMOLDI MG BRICARELLI FD
Citation: M. Grasso et al., PRENATAL-DIAGNOSIS OF 30 FETUSES AT RISK FOR FRAGILE-X-SYNDROME, American journal of medical genetics, 64(1), 1996, pp. 187-190

Authors: BRICARELLI FD PERRONI L PIERLUIG M BARGIACCHI S ARGUSTI A BALDI M PERFUMO G EGEO A CICCOLALLO L STRIGINI P
Citation: Fd. Bricarelli et al., ORIGIN OF CHROMOSOME-21 NONDISJUNCTION - AN ITALIAN STUDY AND EPIDEMIOLOGIC COMPARISONS, American journal of human genetics, 53(3), 1993, pp. 1645-1645

Authors: STRIGINI P PIERLUIGI M BARGIACCHI S PERFUMO C ARGUSTI A HEOUAINE A BRICARELLI FD PAOLUCCI G
Citation: P. Strigini et al., GENETIC EPIDEMIOLOGY OF TRANSIENT LEUKEMIA AND ACUTE-LEUKEMIA IN DOWN-SYNDROME, American journal of human genetics, 53(3), 1993, pp. 1664-1664
Risultati: 1-12 |