Anmelden/Registrieren
Erscheinungsjahr:
 
Zurück zur geteilten Ansicht
Orsetta Zuffardi

Veröffentlichungen von Orsetta Zuffardi zu Zuffardi, Orsetta ->
weitere Veröffentlichungen von Orsetta Zuffardi:
Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human y chromosome long arm (1976)
Gene mapping and serendipity. The locus for torticollis, keloids, cryptorchidism and renal dysplasia (31430, McKusick) is at Xq28, distal to the G6PD locus (1982)
The Cd technique identifies a specific structure related to centromeric function (1984)
Regional assignment of the gene coding for a human Graves' disease autoantigen to 10q21.3–q22.1 (1993)
Indirect immunofluorescence of inactive centromeres as indicator of centromeric function (1986)
A dominantly inherited syndrome (microcephaly, short stature, peculiar facies, mental retardation) associated with two balanced rearrangements involving chromosomes 2;7 and 5;20 (1988)
Evidence for an ancestral alphoid domain on the long arm of human chromosome 2 (1992)
CENP-G in neocentromeres and inactive centromeres (2000)
Changes in the fluorescence patterns of translocated Y chromosome segments in Drosophila melanogaster (1971)
“Jumping” satellites in three generations: A warning for paternity tests and prenatal diagnosis (1976)
Trisomy 16q21»qter (1980)
Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant aicardi's syndrome) in a girl with balanced X/3 translocation (1982)
Deletion of specific sequences or modification of centromeric chromatin are responsible for Y chromosome centromere inactivation (1990)
Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instability (1993)
Are the nail-patella syndrome and the autosomal Goltz-like syndrome the phenotypic expressions of different alleles at the COL5A1 locus? (1993)
Veröffentlichungen zu Zuffardi, Orsetta
Zurück zur geteilten Ansicht
Verfasser Titel Jahr absteigend sortierenaufsteigend sortieren
zeige Details
1
Tiepolo, L., Zuffardi, Orsetta Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human y chromosome long arm
in: Human genetics , ISSN 1432-1203, Vol. 34 (2. 1976), p. 119-124
Zugang: zum Volltext
ähnliche Vorschläge
1976
zeige Details
2
Zuffardi, Orsetta, Fraccaro, M. Gene mapping and serendipity. The locus for torticollis, keloids, cryptorchidism and renal dysplasia (31430, McKusick) is at Xq28, distal to the G6PD locus
in: Human genetics , ISSN 1432-1203, Vol. 62 (3. 1982), p. 280-281
Zugang: zum Volltext
ähnliche Vorschläge
1982
zeige Details
3
Lambiase, Simonetta, Maraschio, Paola, ... The Cd technique identifies a specific structure related to centromeric function
in: Human genetics , ISSN 1432-1203, Vol. 67 (2. 1984), p. 214-215
Zugang: zum Volltext
ähnliche Vorschläge
1984
zeige Details
4
Rossi, Elena, Zarrilli, Raffaele, ... Regional assignment of the gene coding for a human Graves' disease autoantigen to 10q21.3–q22.1
in: Human genetics , ISSN 1432-1203, Vol. 90 (6. 1993), p. 653-654
Zugang: zum Volltext
ähnliche Vorschläge
1993
zeige Details
5
Peretti, Diletta, Maraschio, Paola, ... Indirect immunofluorescence of inactive centromeres as indicator of centromeric function
in: Human genetics , ISSN 1432-1203, Vol. 73 (1. 1986), p. 12-16
Zugang: zum Volltext
ähnliche Vorschläge
1986
zeige Details
6
Vivarelli, Rossella, Zuffardi, Orsetta, ... A dominantly inherited syndrome (microcephaly, short stature, peculiar facies, mental retardation) associated with two balanced rearrangements involving chromosomes 2;7 and 5;20
in: Human genetics , ISSN 1432-1203, Vol. 79 (4. 1988), p. 385-388
Zugang: zum Volltext
ähnliche Vorschläge
1988
zeige Details
7
Avarello, Rosamaria, Pedicini, Antonio, ... Evidence for an ancestral alphoid domain on the long arm of human chromosome 2
in: Human genetics , ISSN 1432-1203, Vol. 89 (2. 1992), p. 247-249
Zugang: zum Volltext
ähnliche Vorschläge
1992
zeige Details
8
Gimelli, Giorgio, Zuffardi, Orsetta, ... CENP-G in neocentromeres and inactive centromeres
in: Chromosoma , ISSN 1432-0886, Vol. 109 (5. 2000), p. 328-333
Zugang: zum Volltext
ähnliche Vorschläge
2000
zeige Details
9
Zuffardi, Orsetta, Tiepolo, L., ... Changes in the fluorescence patterns of translocated Y chromosome segments in Drosophila melanogaster
in: Chromosoma , ISSN 1432-0886, Vol. 34 (3. 1971), p. 274-280
Zugang: zum Volltext
ähnliche Vorschläge
1971
zeige Details
10
Gimelli, G., Porro, E., ... “Jumping” satellites in three generations: A warning for paternity tests and prenatal diagnosis
in: Human genetics , ISSN 1432-1203, Vol. 34 (3. 1976), p. 315-318
Zugang: zum Volltext
ähnliche Vorschläge
1976
zeige Details
11
Garau, Angiolina, Crisponi, G., ... Trisomy 16q21»qter
in: Human genetics , ISSN 1432-1203, Vol. 53 (2. 1980), p. 165-167
Zugang: zum Volltext
ähnliche Vorschläge
1980
zeige Details
12
Ropers, H. H., Zuffardi, Orsetta, ... Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant aicardi's syndrome) in a girl with balanced X/3 translocation
in: Human genetics , ISSN 1432-1203, Vol. 61 (4. 1982), p. 364-368
Zugang: zum Volltext
ähnliche Vorschläge
1982
zeige Details
13
Maraschio, Paola, Zuffardi, Orsetta, ... Deletion of specific sequences or modification of centromeric chromatin are responsible for Y chromosome centromere inactivation
in: Human genetics , ISSN 1432-1203, Vol. 85 (5. 1990), p. 491-494
Zugang: zum Volltext
ähnliche Vorschläge
1990
zeige Details
14
Pezzolo, Annalisa, Gimelli, Giorgio, ... Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instability
in: Human genetics , ISSN 1432-1203, Vol. 92 (1. 1993), p. 23-27
Zugang: zum Volltext
ähnliche Vorschläge
1993
zeige Details
15
Ghiggeri, GianMarco, Caridi, Gianluca, ... Are the nail-patella syndrome and the autosomal Goltz-like syndrome the phenotypic expressions of different alleles at the COL5A1 locus?
in: Human genetics , ISSN 1432-1203, Vol. 91 (2. 1993), p. 175-177
Zugang: zum Volltext
ähnliche Vorschläge
1993
zeige Details
16
Salvadori, Susanna, Deiana, AnnaMaria, ... Colocalization of (TTAGGG)n telomeric sequences and ribosomal genes in Atlantic eels
in: Chromosome research , ISSN 1573-6849, Vol. 3 (1. 1995), p. 54-58
Zugang: zum Volltext
ähnliche Vorschläge
1995
zeige Details
17
Maraschio, Paola, Tupler, Rossella, ... A novel mechanism for the origin of supernumerary marker chromosomes
in: Human genetics , ISSN 1432-1203, Vol. 97 (3. 1996), p. 382-386
Zugang: zum Volltext
ähnliche Vorschläge
1996
zeige Details
18
Maraschio, Paola, Tupler, Rossella, ... A novel mechanism for the origin of supernumerary marker chromosomes
in: Human genetics , ISSN 1432-1203, Vol. 97 (3. 1996), p. 382-386
Zugang: zum Volltext
ähnliche Vorschläge
1996
zeige Details
19
Floridia, Giovanna, Gimelli, Giorgio, ... A neocentromere in the DAZ region of the human Y chromosome
in: Chromosoma , ISSN 1432-0886, Vol. 109 (5. 2000), p. 318-327
Zugang: zum Volltext
ähnliche Vorschläge
2000
zeige Details
20
Curto, F. Lo, Maraschio, Paola, ... The syndrome of partial trisomy 14q
in: European journal of pediatrics , ISSN 1432-1076, Vol. 123 (4. 1976), p. 237-241
Zugang: zum Volltext
ähnliche Vorschläge
1976