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A Sensi

Showing results (11-20 of 52) with videos related to

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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 translocationsF Gualandi, A Sensi, C Trabanelli, et al.
Human Heredity|September 1, 1994
Heteromorphic variant 18ph+ analyzed by sequential CBG and fluorescence in situ hybridizationA 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-FISHA 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 familyA 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 hybridizationA Bonfatti, C Giunta, A Sensi, et al.
European Heart Journal|December 1, 1995
Atrial septal defect type Ostium secundum with and without prolonged atrioventricular conductionG 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 aetiologyP Prontera, F Escande, G Cocchi, et al.
Prenatal Diagnosis|March 12, 1999
Prenatal exclusion of UPD from cytogenetic slides: a simple methodF 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.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 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 translocationsF Gualandi, A Sensi, C Trabanelli, et al.
Human Heredity|September 1, 1994
Heteromorphic variant 18ph+ analyzed by sequential CBG and fluorescence in situ hybridizationA 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-FISHA 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 familyA 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 hybridizationA Bonfatti, C Giunta, A Sensi, et al.
European Heart Journal|December 1, 1995
Atrial septal defect type Ostium secundum with and without prolonged atrioventricular conductionG 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 aetiologyP Prontera, F Escande, G Cocchi, et al.
Prenatal Diagnosis|March 12, 1999
Prenatal exclusion of UPD from cytogenetic slides: a simple methodF 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.
Pageof 6