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Prenatal Diagnosis
|
January 1, 1995
De novo deletions of the 5q13 region and prenatal diagnosis of spinal muscular atrophy
F Capon, S Lo Cicero, C Levato, et al.
Genetic Testing
|
May 5, 2001
A single strand conformation polymorphism-based carrier test for spinal muscular atrophy
S Semprini, A Tacconelli, F Capon, et al.
European Journal of Human Genetics : EJHG
|
October 20, 2000
Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3
F Sangiuolo, E Bruscia, F Capon, et al.
Prenatal Diagnosis
|
June 1, 1994
First-trimester prenatal diagnosis of spinal muscular atrophy using microsatellite markers
S Lo Cicero, F Capon, S Melchionda, et al.
Journal of Medical Genetics
|
March 1, 1995
Neonatal spinal muscular atrophy with diaphragmatic paralysis is unlinked to 5q11.2-q13
G Novelli, F Capon, L Tamisari, et al.
Muscle & Nerve
|
March 1, 1996
Deletion analysis of SMN and NAIP genes in spinal muscular atrophy Italian families
F Capon, C Levato, S Semprini, et al.
Molecular and Cellular Probes
|
June 1, 1993
A tool for the molecular analysis of an early lethal disease: slide-PCR in spinal muscular atrophy patients
F Capon, S Melchionda, M Gennarelli, et al.
American Journal of Human Genetics
|
July 27, 1999
Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22
M Mangino, O Sanchez, I Torrente, et al.
Biochemical and Biophysical Research Communications
|
August 4, 1995
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients
M Gennarelli, M Lucarelli, F Capon, et al.
Cryobiology
|
May 23, 1998
A comparative study of cryogenic lesions in organ-cultured human skin and in reconstituted human skin equivalent
F Capon, M P Cambie-Vanderschelden, V Salmon-Ehr, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 42) with videos related to
Sort By:
Page
of 5
Prenatal Diagnosis
|
January 1, 1995
De novo deletions of the 5q13 region and prenatal diagnosis of spinal muscular atrophy
F Capon, S Lo Cicero, C Levato, et al.
Genetic Testing
|
May 5, 2001
A single strand conformation polymorphism-based carrier test for spinal muscular atrophy
S Semprini, A Tacconelli, F Capon, et al.
European Journal of Human Genetics : EJHG
|
October 20, 2000
Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3
F Sangiuolo, E Bruscia, F Capon, et al.
Prenatal Diagnosis
|
June 1, 1994
First-trimester prenatal diagnosis of spinal muscular atrophy using microsatellite markers
S Lo Cicero, F Capon, S Melchionda, et al.
Journal of Medical Genetics
|
March 1, 1995
Neonatal spinal muscular atrophy with diaphragmatic paralysis is unlinked to 5q11.2-q13
G Novelli, F Capon, L Tamisari, et al.
Muscle & Nerve
|
March 1, 1996
Deletion analysis of SMN and NAIP genes in spinal muscular atrophy Italian families
F Capon, C Levato, S Semprini, et al.
Molecular and Cellular Probes
|
June 1, 1993
A tool for the molecular analysis of an early lethal disease: slide-PCR in spinal muscular atrophy patients
F Capon, S Melchionda, M Gennarelli, et al.
American Journal of Human Genetics
|
July 27, 1999
Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22
M Mangino, O Sanchez, I Torrente, et al.
Biochemical and Biophysical Research Communications
|
August 4, 1995
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients
M Gennarelli, M Lucarelli, F Capon, et al.
Cryobiology
|
May 23, 1998
A comparative study of cryogenic lesions in organ-cultured human skin and in reconstituted human skin equivalent
F Capon, M P Cambie-Vanderschelden, V Salmon-Ehr, et al.
Page
of 5