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Bollettino Della Societa Italiana Di Biologia Sperimentale
|
October 30, 1983
[Microcytological characteristics of reticulocytes in heterozygous beta-thalassemia]
G Castaldi, G Camerini, A Sensi, et al.
Prenatal Diagnosis
|
June 22, 2000
Prenatal UPD testing survey in Robertsonian translocations
F Gualandi, A Sensi, C Trabanelli, et al.
Human Heredity
|
September 1, 1994
Heteromorphic variant 18ph+ analyzed by sequential CBG and fluorescence in situ hybridization
A Sensi, C Giunta, A Bonfatti, et al.
European Journal of Histochemistry : EJH
|
January 1, 1995
Syntenic groups between human chromosome 9 and Indian muntjac chromosomes revealed by ZOO-FISH
A Sensi, R Gruppioni, A Bonfatti, et al.
Clinical Genetics
|
June 1, 1996
Branchio-oto (BO) syndrome and oculo-auriculo-vertebral phenotype: overlapping clinical findings in a child from a BO family
A Sensi, G Cocchi, A Martini, et al.
European Journal of Histochemistry : EJH
|
January 1, 1993
Heteromorphism of human chromosome 18 detected by fluorescent in situ hybridization
A Bonfatti, C Giunta, A Sensi, et al.
European Heart Journal
|
December 1, 1995
Atrial septal defect type Ostium secundum with and without prolonged atrioventricular conduction
G Bosi, A Sensi, M Scorrano, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 26, 2009
An intermediate phenotype between Hay-Wells and Rapp-Hodgkin syndromes in a patient with a novel P63 mutation: confirmation of a variable phenotypic spectrum with a common aetiology
P Prontera, F Escande, G Cocchi, et al.
Prenatal Diagnosis
|
March 12, 1999
Prenatal exclusion of UPD from cytogenetic slides: a simple method
F Gualandi, A Sensi, O Calabrese, et al.
Genetic Counseling (Geneva, Switzerland)
|
March 23, 2007
FGFR3 mutation in thanatophoric dysplasia type 1 with bilateral cystic renal dysplasia: coincidence or a new association?
P Prontera, A Sensi, G Pilu, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 52) with videos related to
Sort By:
Page
of 6
Bollettino Della Societa Italiana Di Biologia Sperimentale
|
October 30, 1983
[Microcytological characteristics of reticulocytes in heterozygous beta-thalassemia]
G Castaldi, G Camerini, A Sensi, et al.
Prenatal Diagnosis
|
June 22, 2000
Prenatal UPD testing survey in Robertsonian translocations
F Gualandi, A Sensi, C Trabanelli, et al.
Human Heredity
|
September 1, 1994
Heteromorphic variant 18ph+ analyzed by sequential CBG and fluorescence in situ hybridization
A Sensi, C Giunta, A Bonfatti, et al.
European Journal of Histochemistry : EJH
|
January 1, 1995
Syntenic groups between human chromosome 9 and Indian muntjac chromosomes revealed by ZOO-FISH
A Sensi, R Gruppioni, A Bonfatti, et al.
Clinical Genetics
|
June 1, 1996
Branchio-oto (BO) syndrome and oculo-auriculo-vertebral phenotype: overlapping clinical findings in a child from a BO family
A Sensi, G Cocchi, A Martini, et al.
European Journal of Histochemistry : EJH
|
January 1, 1993
Heteromorphism of human chromosome 18 detected by fluorescent in situ hybridization
A Bonfatti, C Giunta, A Sensi, et al.
European Heart Journal
|
December 1, 1995
Atrial septal defect type Ostium secundum with and without prolonged atrioventricular conduction
G Bosi, A Sensi, M Scorrano, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 26, 2009
An intermediate phenotype between Hay-Wells and Rapp-Hodgkin syndromes in a patient with a novel P63 mutation: confirmation of a variable phenotypic spectrum with a common aetiology
P Prontera, F Escande, G Cocchi, et al.
Prenatal Diagnosis
|
March 12, 1999
Prenatal exclusion of UPD from cytogenetic slides: a simple method
F Gualandi, A Sensi, O Calabrese, et al.
Genetic Counseling (Geneva, Switzerland)
|
March 23, 2007
FGFR3 mutation in thanatophoric dysplasia type 1 with bilateral cystic renal dysplasia: coincidence or a new association?
P Prontera, A Sensi, G Pilu, et al.
Page
of 6