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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
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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
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ähnliche Vorschläge 		1976
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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
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ähnliche Vorschläge 		1982
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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
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ähnliche Vorschläge 		1984
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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
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ähnliche Vorschläge 		1993
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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
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ähnliche Vorschläge 		1986
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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
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ähnliche Vorschläge 		1988
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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
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ähnliche Vorschläge 		1992
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8 		Gimelli, Giorgio, Zuffardi, Orsetta, ... CENP-G in neocentromeres and inactive centromeres
in: Chromosoma , ISSN 1432-0886, Vol. 109 (5. 2000), p. 328-333
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ähnliche Vorschläge 		2000
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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
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ähnliche Vorschläge 		1971
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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
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ähnliche Vorschläge 		1976
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11 		Garau, Angiolina, Crisponi, G., ... Trisomy 16q21»qter
in: Human genetics , ISSN 1432-1203, Vol. 53 (2. 1980), p. 165-167
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ähnliche Vorschläge 		1980
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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
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ähnliche Vorschläge 		1982
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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
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ähnliche Vorschläge 		1990
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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
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ähnliche Vorschläge 		1993
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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
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ähnliche Vorschläge 		1993
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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
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ähnliche Vorschläge 		1995
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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
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ähnliche Vorschläge 		1996
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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
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ähnliche Vorschläge 		1996
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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
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ähnliche Vorschläge 		2000
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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
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ähnliche Vorschläge 		1976