AAAAAA

   
Results: 1-15 |
Results: 15
IN-VITRO REACTIVATION OF THE FMR1 GENE INVOLVED IN FRAGILE-X-SYNDROME
Authors: CHIURAZZI P POMPONI MG WILLEMSEN R OOSTRA BA NERI G
Citation: P. Chiurazzi et al., IN-VITRO REACTIVATION OF THE FMR1 GENE INVOLVED IN FRAGILE-X-SYNDROME, Human molecular genetics, 7(1), 1998, pp. 109-113
SMT3A, A HUMAN HOMOLOG OF THE S-CEREVISIAE-SMT3 GENE, MAPS TO CHROMOSOME-21QTER AND DEFINES A NOVEL GENE FAMILY
Authors: LAPENTA V CHIURAZZI P VANDERSPEK P PIZZUTI A HANAOKA F BRAHE C
Citation: V. Lapenta et al., SMT3A, A HUMAN HOMOLOG OF THE S-CEREVISIAE-SMT3 GENE, MAPS TO CHROMOSOME-21QTER AND DEFINES A NOVEL GENE FAMILY, Genomics, 40(2), 1997, pp. 362-366
A HUMAN HOMOLOG OF THE SACCHAROMYCES-CEREVISIAE SMT3 GENE MAPS TO THETELOMERIC REGION OF 21Q
Authors: LAPENTA V CHIURAZZI P VANDERSPEK P PIZZUTI A BRAHE C
Citation: V. Lapenta et al., A HUMAN HOMOLOG OF THE SACCHAROMYCES-CEREVISIAE SMT3 GENE MAPS TO THETELOMERIC REGION OF 21Q, Cytogenetics and cell genetics, 77, 1997, pp. 13-13
IN-VITRO REACTIVATION OF THE FRAGILE-X-SYNDROME GENE
Authors: CHIURAZZI P POMPONI MG WILLEMSEN R OOSTRA BA NERI G
Citation: P. Chiurazzi et al., IN-VITRO REACTIVATION OF THE FRAGILE-X-SYNDROME GENE, American journal of human genetics, 61(4), 1997, pp. 1786-1786
XLMR GENES - UPDATE 1996
Authors: LUBS HA CHIURAZZI P ARENA JF SCHWARTZ C TRANEBJAERG L NERI G
Citation: Ha. Lubs et al., XLMR GENES - UPDATE 1996, American journal of medical genetics, 64(1), 1996, pp. 147-157
SIGNIFICANCE OF LINKAGE DISEQUILIBRIUM BETWEEN THE FRAGILE-X LOCUS AND ITS FLANKING MARKERS
Authors: CHIURAZZI P MACPHERSON J SHERMAN S NERI G
Citation: P. Chiurazzi et al., SIGNIFICANCE OF LINKAGE DISEQUILIBRIUM BETWEEN THE FRAGILE-X LOCUS AND ITS FLANKING MARKERS, American journal of medical genetics, 64(1), 1996, pp. 203-208
FRAGILE-X FOUNDER CHROMOSOMES IN ITALY - A FEW INITIAL EVENTS AND POSSIBLE EXPLANATION FOR THEIR HETEROGENEITY
Authors: CHIURAZZI P GENUARDI M KOZAK L GIOVANNUCCIUZIELLI ML BUSSANI C DAGNABRICARELLI F GRASSO M PERRONI L SEBASTIO G SPERANDEO MP OOSTRA BA NERI G
Citation: P. Chiurazzi et al., FRAGILE-X FOUNDER CHROMOSOMES IN ITALY - A FEW INITIAL EVENTS AND POSSIBLE EXPLANATION FOR THEIR HETEROGENEITY, American journal of medical genetics, 64(1), 1996, pp. 209-215
EXTENDED GENE DIVERSITY AT TIRE FMR1 LOCUS AND NEIGHBORING CA REPEATSIN A SUB-SAHARAN POPULATION
Authors: CHIURAZZI P DESTROBISOL G GENUARDI M OOSTRA BA SPEDINI G NERI G
Citation: P. Chiurazzi et al., EXTENDED GENE DIVERSITY AT TIRE FMR1 LOCUS AND NEIGHBORING CA REPEATSIN A SUB-SAHARAN POPULATION, American journal of medical genetics, 64(1), 1996, pp. 216-219
DICENTRIC CHROMOSOME-Y ASSOCIATED WITH LEYDIG-CELL AGENESIS AND SEX REVERSAL
Authors: GENUARDI M BARDONI B FLORIDIA G CHIURAZZI P SCARANO G ZOLLINO M GARCEA N MARTININERI ME NERI G
Citation: M. Genuardi et al., DICENTRIC CHROMOSOME-Y ASSOCIATED WITH LEYDIG-CELL AGENESIS AND SEX REVERSAL, Clinical genetics, 47(1), 1995, pp. 38-41
FRAGILE-X SYNDROME - ROUNDER CHROMOSOMES IN ITALY
Authors: CHIURAZZI P KOZAK L GENUARDI M GIOVANNUCCIUZIELLI ML BUSSANI C DAGNABRICARELLI F GRASSO M PERRONE L SEBASTIO G SPERANDEO MP OOSTRA BA NERI G
Citation: P. Chiurazzi et al., FRAGILE-X SYNDROME - ROUNDER CHROMOSOMES IN ITALY, American journal of human genetics, 57(4), 1995, pp. 919-919
NO APPARENT INVOLVEMENT OF THE FMR1 GENE IN 5 PATIENTS WITH PHENOTYPIC MANIFESTATIONS OF THE FRAGILE-X-SYNDROME
Authors: CHIURAZZI P DEGRAAFF E NG J VERKERK AJMH WOLFSON S FISCH GS KOZAK L NERI G OOSTRA BA
Citation: P. Chiurazzi et al., NO APPARENT INVOLVEMENT OF THE FMR1 GENE IN 5 PATIENTS WITH PHENOTYPIC MANIFESTATIONS OF THE FRAGILE-X-SYNDROME, American journal of medical genetics, 51(4), 1994, pp. 309-314
UNSTABLE TRIPLETS AND THEIR MUTATIONAL MECHANISM - SIZE-REDUCTION OF THE CGG REPEAT VS GERMLINE MOSAICISM IN THE FRAGILE-X-SYNDROME
Authors: CHIURAZZI P KOZAK L NERI G
Citation: P. Chiurazzi et al., UNSTABLE TRIPLETS AND THEIR MUTATIONAL MECHANISM - SIZE-REDUCTION OF THE CGG REPEAT VS GERMLINE MOSAICISM IN THE FRAGILE-X-SYNDROME, American journal of medical genetics, 51(4), 1994, pp. 517-521
XLMR GENES - UPDATE 1994
Authors: NERI G CHIURAZZI P ARENA JF LUBS HA
Citation: G. Neri et al., XLMR GENES - UPDATE 1994, American journal of medical genetics, 51(4), 1994, pp. 542-549
EXCLUSION OF LINKAGE BETWEEN AUTOSOMAL-DOMINANT SPLIT HAND SPLIT FOOTAND MARKERS FROM CHROMOSOME 7Q - FURTHER EVIDENCE FOR GENETIC-HETEROGENEITY
Authors: GURRIERI F GENUARDI M CHIURAZZI P GILLESSENKAESBACH G NERI G
Citation: F. Gurrieri et al., EXCLUSION OF LINKAGE BETWEEN AUTOSOMAL-DOMINANT SPLIT HAND SPLIT FOOTAND MARKERS FROM CHROMOSOME 7Q - FURTHER EVIDENCE FOR GENETIC-HETEROGENEITY, American journal of human genetics, 55(4), 1994, pp. 853-855
MAPPING OF A GENE FOR NONSPECIFIC X-LINKED MENTAL-RETARDATION - EVIDENCE FOR LINKAGE TO CHROMOSOMAL REGION XP21.1-XP22.3
Authors: KOZAK L CHIURAZZI P GENUARDI M POMPONI MG ZOLLINO M NERI G
Citation: L. Kozak et al., MAPPING OF A GENE FOR NONSPECIFIC X-LINKED MENTAL-RETARDATION - EVIDENCE FOR LINKAGE TO CHROMOSOMAL REGION XP21.1-XP22.3, Journal of Medical Genetics, 30(10), 1993, pp. 866-869
Risultati: 1-15 |