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Results of search for 'au:"Turco, A E"', page 1 of 2
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Authors
Barker, D F
Biasi, M O
Bresin, E
Carbonara, A
Chiaffoni, G P
Corrà, S
De Marchi, M
De Prisco, O
Dietz-Band, J N
Englisch, S
Gammaro, L
Maschio, G
Padovani, E M
Peissel, B
Pignatti, P F
Renieri, A
Restagno, G
Rossetti, S
Skolnick, M H
Turco, A E
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Topics
Adolescent
Adult
Chromosome Mapping
DNA
Female
Genetic Linkage
Humans
Italy
Male
Middle Aged
Mutation
Nephritis, Hereditary
Pedigree
Polycystic Kidney, Autosomal Dominant
Polymerase Chain Reaction
Pregnancy
Proteins
TRPP Cation Channels
diagnosis
genetics
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English
Your search returned 29 results.
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1.
Genetics and nephro-uropathies.
[electronic resource]
by
Turco, A E
Producer:
20021220
In:
La Pediatria medica e chirurgica : Medical and surgical pediatrics
vol. 24
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2.
Pregnancy, microchimerism and autoimmunity: an update.
[electronic resource]
by
Turco, A E
Bambara, L M
Producer:
20041231
In:
Lupus
vol. 13
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3.
Tracking disease genes by reverse genetics.
[electronic resource]
by
Pignatti, P F
Turco, A E
Producer:
19930226
In:
Journal of psychiatric research
vol. 26
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4.
Autosomal dominant polycystic kidney disease: clinical and genetic aspects.
[electronic resource]
by
Sessa, A
Ghiggeri, G M
Turco, A E
Producer:
19980226
In:
Journal of nephrology
vol. 10
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5.
Alport syndrome--is there a genotype-phenotype relationship?
[electronic resource]
by
Turco, A E
Renieri, A
De Marchi, M
Producer:
19971009
In:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
vol. 12
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6.
Erroneous genetic risk assessment of Alport syndrome.
[electronic resource]
by
Turco, A E
Rossetti, S
Bresin, E
Corrá, S
Producer:
19951213
In:
Lancet (London, England)
vol. 346
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7.
Rapid DNA-based prenatal diagnosis of autosomal dominant polycystic kidney disease.
[electronic resource]
by
Turco, A E
Peissel, B
Rossetti, S
Pignatti, P F
Producer:
19941026
In:
Archives of pediatrics & adolescent medicine
vol. 148
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8.
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP).
[electronic resource]
by
Rossato, M
Rigotti, M
Grazia, M
Turco, A E
Bonomi, L
Producer:
19970121
In:
Acta ophthalmologica Scandinavica
vol. 74
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9.
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene.
[electronic resource]
by
Turco, A E
Clementi, M
Rossetti, S
Tenconi, R
Pignatti, P F
Producer:
19970609
In:
American journal of kidney diseases : the official journal of the National Kidney Foundation
vol. 28
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10.
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA).
[electronic resource]
by
Rossetti, S
Englisch, S
Bresin, E
Pignatti, P F
Turco, A E
Producer:
19970724
In:
Molecular and cellular probes
vol. 11
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11.
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genes.
[electronic resource]
by
Rossetti, S
Corrà, S
Biasi, M O
Turco, A E
Pignatti, P F
Producer:
19951130
In:
Molecular and cellular probes
vol. 9
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12.
Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's syndrome.
[electronic resource]
by
Turco, A E
Bresin, E
Rossetti, S
Peterlin, B
Morandi, R
Pignatti, P F
Producer:
19970903
In:
American journal of kidney diseases : the official journal of the National Kidney Foundation
vol. 30
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13.
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1).
[electronic resource]
by
Bresin, E
Rossetti, S
Englisch, S
Corrà, S
Pignatti, P F
Turco, A E
Producer:
19970403
In:
Molecular and cellular probes
vol. 10
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14.
Three novel mutations of the PKD1 gene in Italian families with autosomal dominant polycystic kidney disease.
[electronic resource]
by
Turco, A E
Rossetti, S
Bresin, E
Englisch, S
Corrà, S
Pignatti, P F
Producer:
19970930
In:
Human mutation
vol. 10
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15.
Clinical applications of genetic linkage analysis for the molecular diagnostics of ADPKD, using DNA markers linked to the PKD1 and PKD2 genes.
[electronic resource]
by
Turco, A E
Rossetti, S
Peissel, B
Gammaro, L
Maschio, G
Pignatti, P F
Producer:
19960327
In:
Contributions to nephrology
vol. 115
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16.
A novel nonsense mutation in the PKD1 gene (C3817T) is associated with autosomal dominant polycystic kidney disease (ADPKD) in a large three-generation Italian family.
[electronic resource]
by
Turco, A E
Rossetti, S
Bresin, E
Corra, S
Gammaro, L
Maschio, G
Pignatti, P F
Producer:
19951215
In:
Human molecular genetics
vol. 4
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17.
Skeletal malformations and polycystic kidney disease.
[electronic resource]
by
Turco, A E
Peissel, B
Rossetti, S
Pignatti, P F
Padovani, E M
Chiaffoni, G P
Producer:
19950209
In:
Journal of medical genetics
vol. 31
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18.
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers.
[electronic resource]
by
Dietz-Band, J N
Turco, A E
Willard, H F
Vincent, A
Skolnick, M H
Barker, D F
Producer:
19910213
In:
Cytogenetics and cell genetics
vol. 54
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19.
Autosomal dominant polycystic kidney disease (ADPKD) in an Italian family carrying a novel nonsense mutation and two missense changes in exons 44 and 45 of the PKD1 Gene.
[electronic resource]
by
Rossetti, S
Bresin, E
Restagno, G
Carbonara, A
Corrà, S
De Prisco, O
Pignatti, P F
Turco, A E
Producer:
19970219
In:
American journal of medical genetics
vol. 65
Online resources:
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20.
Gene linkage analysis and DNA based detection of autosomal dominant polycystic kidney disease (ADPKD) in a newborn infant. Case report.
[electronic resource]
by
Turco, A E
Padovani, E M
Peissel, B
Chiaffoni, G P
Rossetti, S
Gammaro, L
Maschio, G
Pignatti, P F
Producer:
19960307
In:
Journal of perinatal medicine
vol. 23
Online resources:
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