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B Dallapiccola

Showing results (131-140 of 312) with videos related to

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Genetic Testing|May 5, 2001
A single strand conformation polymorphism-based carrier test for spinal muscular atrophyS Semprini, A Tacconelli, F Capon, et al.
Prenatal Diagnosis|August 1, 1993
On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndromeG Martini, G Carillo, F Catizone, et al.
Journal of Medical Genetics|December 1, 1984
A live infant with trisomy 14 mosaicism and nuclear abnormalities of the neutrophilsB Dallapiccola, G Ferranti, A Giannotti, et al.
Journal of Medical Genetics|August 1, 1980
Segregation of an X ring chromosome in two generationsB Dallapiccola, L Bruni, B Boscherini, et al.
The American Journal of Cardiology|June 15, 1996
Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresiaM C Digilio, B Marino, S Grazioli, et al.
Prenatal Diagnosis|June 1, 1994
First-trimester prenatal diagnosis of spinal muscular atrophy using microsatellite markersS Lo Cicero, F Capon, S Melchionda, et al.
Prenatal Diagnosis|July 1, 1981
The possibility of prenatal diagnosis by gene dosage: confirmation of duplication 10q24 to qter from GOT-1 activity in fetal erythrocytesB Dallapiccola, A Pachì, G Ferranti, et al.
Human Heredity|December 22, 1998
A novel mutation (R271X) in the myotubularin gene causes a severe miotubular myopathyA De Luca, I Torrente, M Mangino, et al.
Human Genetics|September 1, 1990
Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF familiesG Novelli, P Gasparini, A Savoia, et al.
Journal of Human Genetics|February 4, 1999
A single-nucleotide polymorphism in the human bone morphogenetic protein-4 (BMP 4) geneM Mangino, I Torrente, A De Luca, et al.
Pageof 32

Showing results (131-140 of 312) with videos related to

Sort By:
Pageof 32
Genetic Testing|May 5, 2001
A single strand conformation polymorphism-based carrier test for spinal muscular atrophyS Semprini, A Tacconelli, F Capon, et al.
Prenatal Diagnosis|August 1, 1993
On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndromeG Martini, G Carillo, F Catizone, et al.
Journal of Medical Genetics|December 1, 1984
A live infant with trisomy 14 mosaicism and nuclear abnormalities of the neutrophilsB Dallapiccola, G Ferranti, A Giannotti, et al.
Journal of Medical Genetics|August 1, 1980
Segregation of an X ring chromosome in two generationsB Dallapiccola, L Bruni, B Boscherini, et al.
The American Journal of Cardiology|June 15, 1996
Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresiaM C Digilio, B Marino, S Grazioli, et al.
Prenatal Diagnosis|June 1, 1994
First-trimester prenatal diagnosis of spinal muscular atrophy using microsatellite markersS Lo Cicero, F Capon, S Melchionda, et al.
Prenatal Diagnosis|July 1, 1981
The possibility of prenatal diagnosis by gene dosage: confirmation of duplication 10q24 to qter from GOT-1 activity in fetal erythrocytesB Dallapiccola, A Pachì, G Ferranti, et al.
Human Heredity|December 22, 1998
A novel mutation (R271X) in the myotubularin gene causes a severe miotubular myopathyA De Luca, I Torrente, M Mangino, et al.
Human Genetics|September 1, 1990
Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF familiesG Novelli, P Gasparini, A Savoia, et al.
Journal of Human Genetics|February 4, 1999
A single-nucleotide polymorphism in the human bone morphogenetic protein-4 (BMP 4) geneM Mangino, I Torrente, A De Luca, et al.
Pageof 32