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Results of search for 'au:"Lenzini, E"', page 1 of 2
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Authors
Anglani, F
Arslanian, A
Artifoni, L
Bacchetta, M
Baccichetti, C
Baroncini, A
Battistella, P A
Benini, F
Bertoli, P
Bricarelli, F D
Carbone, L D
Goppion, G
Lenzini, E
Leszl, A
Marini, A
Mengarda, G
Peserico, A
Piovan, E
Suma, V
Tenconi, R
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Topics
Adolescent
Adult
Child
Child, Preschool
Chromosome Aberrations
Chromosome Banding
Chromosome Disorders
Chromosomes, Human, 6-12 and X
Female
Humans
Infant
Infant, Newborn
Italy
Karyotyping
Male
Pregnancy
Translocation, Genetic
Trisomy
X Chromosome
genetics
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English
Italian
Your search returned 22 results.
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1.
[Genetic counseling in adult-type polycystic disease of the kidney].
[electronic resource]
by
Baccichetti, C
Lenzini, E
Producer:
19860616
In:
Minerva urologica e nefrologica = The Italian journal of urology and nephrology
vol. 37
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2.
Dermatoglyphic pattern of the 9p syndrome.
[electronic resource]
by
Drusini, A
Lenzini, E
Producer:
19850314
In:
Acta anthropogenetica
vol. 7
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3.
Trisomy 8p by malsegregation of a t(5;8)(p15;p11)mat in a case of XY pure gonadal dysgenesis.
[electronic resource]
by
Memo, L
Lenzini, E
Baccichetti, C
Producer:
19890322
In:
Annales de genetique
vol. 31
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4.
Down syndrome in the Belluno district (Veneto region, northeast Italy): age distribution and morbidity.
[electronic resource]
by
Baccichetti, C
Lenzini, E
Pegoraro, R
Producer:
19910416
In:
American journal of medical genetics. Supplement
vol. 7
Online resources:
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5.
A case of septic miscarriage, a probable complication of chorion villus sampling.
[electronic resource]
by
Marini, A
Suma, V
Baccichetti, C
Lenzini, E
Producer:
19880915
In:
Prenatal diagnosis
vol. 8
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6.
Study on segregation and risk for abnormal offspring in carriers of pericentric inversion of the (p11 leads to q13) segment of chromosome 2.
[electronic resource]
by
Baccichetti, C
Lenzini, E
Peserico, A
Tenconi, R
Producer:
19810317
In:
Clinical genetics
vol. 18
Online resources:
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7.
[Reciprocal translocations associated with phenotypic anomalies. Presentation of 4 cases].
[electronic resource]
by
Lenzini, E
Artifoni, L
Anglani, F
Tenconi, R
Producer:
19800923
In:
Pathologica
vol. 71
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8.
Terminal deletion of the short arm of chromosome 5.
[electronic resource]
by
Baccichetti, C
Lenzini, E
Artifoni, L
Caufin, D
Marangoni, P
Producer:
19890502
In:
Clinical genetics
vol. 34
Online resources:
Available from publisher's website
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9.
Frequency of abnormal karyotypes in relation to the ascertainment method in females referred for suspected sex chromosome abnormality.
[electronic resource]
by
Anglani, F
Baccichetti, C
Artifoni, L
Lenzini, E
Tenconi, R
Producer:
19840521
In:
Clinical genetics
vol. 25
Online resources:
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10.
[Analysis of disaccharidase activity of the amniotic fluid for the early prenatal diagnosis of abnormalities of patency and motility of the fetal intestine].
[electronic resource]
by
Clementi, M
Baccichetti, C
Lucci, G
Lenzini, E
Tenconi, R
Producer:
19860219
In:
Minerva ginecologica
vol. 37
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11.
Spontaneous resolution of cystic hygroma in a 46,XX normal female.
[electronic resource]
by
Baccichetti, C
Lenzini, E
Suma, V
Benini, F
Marini, A
Producer:
19901119
In:
Prenatal diagnosis
vol. 10
Online resources:
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12.
9p trisomy: a new case due to maternal t(9;18) translocation.
[electronic resource]
by
Preto, A
Lenzini, E
Drigo, P
Fasoli, G
De Pascale, A
Producer:
19780724
In:
Acta geneticae medicae et gemellologiae
vol. 26
Online resources:
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13.
Partial duplication of 17 long arm.
[electronic resource]
by
Lenzini, E
Leszl, A
Artifoni, L
Casellato, R
Tenconi, R
Baccichetti, C
Producer:
19890322
In:
Annales de genetique
vol. 31
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14.
[The syndrome of trisomy 9p and presentation of 2 new cases].
[electronic resource]
by
Baccichetti, C
Lenzini, E
Forabosco, A
Baroncini, A
Dordo, B
Mengarda, G
Producer:
19800923
In:
Pathologica
vol. 71
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15.
A new family with extra material on proximal 15q.
[electronic resource]
by
Turolla, L
Baccichetti, C
Artifoni, L
Lenzini, E
Leszl, A
Tenconi, R
Producer:
19900222
In:
Annales de genetique
vol. 32
Availability:
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16.
Hypomelanosis of Ito: involvement of chromosome aberrations in this syndrome.
[electronic resource]
by
Lenzini, E
Bertoli, P
Artifoni, L
Battistella, P A
Baccichetti, C
Peserico, A
Producer:
19911204
In:
Annales de genetique
vol. 34
Availability:
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17.
Replication patterns of human X isochromosomes by high-resolution banding.
[electronic resource]
by
Artifoni, L
Baccichetti, C
Piovan, E
Anglani, F
Lenzini, E
Goppion, G
Tenconi, R
Producer:
19840319
In:
Cytogenetics and cell genetics
vol. 36
Online resources:
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18.
[Reciprocal and Robertsonian translocations in a population selected for suspected chromosome anomalies].
[electronic resource]
by
Lenzini, E
Artifoni, L
Anglani, F
Goppion, G
Piovan, E
Tenconi, R
Baccichetti, C
Producer:
19850205
In:
Pathologica
vol. 75 Suppl
Availability:
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19.
Duplication of an Xp segment that includes the ZFX locus causes sex inversion in man.
[electronic resource]
by
Scherer, G
Schempp, W
Baccichetti, C
Lenzini, E
Bricarelli, F D
Carbone, L D
Wolf, U
Producer:
19890407
In:
Human genetics
vol. 81
Online resources:
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20.
Partial trisomy 9 : clinical and cytogenetic correlations.
[electronic resource]
by
Baccichetti, C
Lenzini, E
Temperani, P
Pallotta, R
Giorgi, P L
Tarantino, E
Mengarda, G
Dordi, B
Producer:
19801027
In:
Annales de genetique
vol. 22
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