ACNP - Italian Periodicals Catalogue

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Results: 1-9 |

Results: 9

SEQUENCE HOMOLOGY BETWEEN 4QTER AND 10QTER LOCI FACILITATES THE INSTABILITY OF SUBTELOMERIC KPNI REPEAT UNITS IMPLICATED IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY

Authors: CACURRI S PIAZZO N DEIDDA G VIGNETI E GALLUZZI G COLANTONI L MERICO B RICCI E FELICETTI L

Citation: S. Cacurri et al., SEQUENCE HOMOLOGY BETWEEN 4QTER AND 10QTER LOCI FACILITATES THE INSTABILITY OF SUBTELOMERIC KPNI REPEAT UNITS IMPLICATED IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY, American journal of human genetics, 63(1), 1998, pp. 181-190

A SIMPLE AND RELIABLE TEST FOR THE MOLECULAR DIAGNOSIS OF FSHD

Authors: RICCI E DEIDDA G CACURRI S GALLUZZI G PIAZZO N MERICO B COLANTONI L DEROSA G SERVIDEI S TONALI P FELICETTI L

Citation: E. Ricci et al., A SIMPLE AND RELIABLE TEST FOR THE MOLECULAR DIAGNOSIS OF FSHD, Neurology, 48(3), 1997, pp. 21002-21002

SEQUENCE HOMOLOGY BETWEEN 4QTER AND 10QTER LOCI FAVORS THE OCCURRENCEOF INTERCHROMOSOMAL EXCHANGES AND THE INSTABILITY OF SUBTELOMERIC KPNL REPEATS IMPLICATED IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD)

Authors: CACURRI S DEIDDA G PIAZZO N GALUZZI G COLANTONI L RICCI E MERICO B FELICETTI L

Citation: S. Cacurri et al., SEQUENCE HOMOLOGY BETWEEN 4QTER AND 10QTER LOCI FAVORS THE OCCURRENCEOF INTERCHROMOSOMAL EXCHANGES AND THE INSTABILITY OF SUBTELOMERIC KPNL REPEATS IMPLICATED IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD), American journal of human genetics, 61(4), 1997, pp. 963-963

DIRECT-DETECTION OF 4Q35 REARRANGEMENTS IMPLICATED IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD)

Authors: DEIDDA G CACURRI S PIAZZO N FELICETTI L

Citation: G. Deidda et al., DIRECT-DETECTION OF 4Q35 REARRANGEMENTS IMPLICATED IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD), Journal of Medical Genetics, 33(5), 1996, pp. 361-365

PHYSICAL MAPPING EVIDENCE FOR A DUPLICATED REGION ON CHROMOSOME 10QTER SHOWING HIGH HOMOLOGY WITH THE FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY LOCUS ON CHROMOSOME 4QTER

Authors: DEIDDA G CACURRI S GRISANTI P VIGNETI E PIAZZO N FELICETTI L

Citation: G. Deidda et al., PHYSICAL MAPPING EVIDENCE FOR A DUPLICATED REGION ON CHROMOSOME 10QTER SHOWING HIGH HOMOLOGY WITH THE FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY LOCUS ON CHROMOSOME 4QTER, European journal of human genetics, 3(3), 1995, pp. 155-167

PHYSICAL MAPPING EVIDENCE FOR A DUPLICATED REGION ON CHROMOSOME 10QTER SHOWING HIGH HOMOLOGY WITH THE FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD) LOCUS ON CHROMOSOME 4QTER

Authors: DEIDDA G CACURRI S GRISANTI P VIGNETI E PIAZZO N FELICETTI L

Citation: G. Deidda et al., PHYSICAL MAPPING EVIDENCE FOR A DUPLICATED REGION ON CHROMOSOME 10QTER SHOWING HIGH HOMOLOGY WITH THE FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD) LOCUS ON CHROMOSOME 4QTER, American journal of human genetics, 57(4), 1995, pp. 1498-1498

4Q35 MOLECULAR PROBES FOR THE DIAGNOSIS AND GENETIC-COUNSELING OF FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY

Authors: DEIDDA GC CACURRI S LACESA I SCOPPETTA C FELICETTI L

Citation: Gc. Deidda et al., 4Q35 MOLECULAR PROBES FOR THE DIAGNOSIS AND GENETIC-COUNSELING OF FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY, Annals of neurology, 36(1), 1994, pp. 117-118

CHROMOSOME 4Q35 HAPLOTYPES AND DNA REARRANGEMENTS SEGREGATING IN AFFECTED SUBJECTS OF 19 ITALIAN FAMILIES WITH FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD)

Authors: CACURRI S DEIDDA G PIAZZO N NOVELLETTO A LACESA I SERVIDEI S GALLUZZI G WIJMENGA C FRANTS RR FELICETTI L

Citation: S. Cacurri et al., CHROMOSOME 4Q35 HAPLOTYPES AND DNA REARRANGEMENTS SEGREGATING IN AFFECTED SUBJECTS OF 19 ITALIAN FAMILIES WITH FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD), Human genetics, 94(4), 1994, pp. 367-374

4Q35 DNA REARRANGEMENTS DETECTED BY PROBE P13E-11 IN THE AFFECTED SUBJECTS OF 15 ITALIAN FAMILIES WITH FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY

Authors: FELICETTI L CACURRI S DEIDDA G PIAZZO N LACESA I GRISANTI P

Citation: L. Felicetti et al., 4Q35 DNA REARRANGEMENTS DETECTED BY PROBE P13E-11 IN THE AFFECTED SUBJECTS OF 15 ITALIAN FAMILIES WITH FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY, American journal of human genetics, 53(3), 1993, pp. 999-999

Risultati: 1-9 |