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Showing results (51-60 of 96) with videos related to
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Muscle & Nerve
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September 1, 1996
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?
M Fanin, M P Freda, L Vitiello, et al.
Nucleic Acids Research
|
October 11, 1994
Single base substitutions are detected by double strand conformation analysis
F A Saad, B Halliger, C R Müller, et al.
Neuroepidemiology
|
January 1, 1995
Frequency of duplication at 17p11.2 in families of northeast Italy with Charcot-Marie-Tooth disease type 1
M L Mostacciuolo, F Schiavon, C Angelini, et al.
Human Molecular Genetics
|
August 1, 1992
A 3' consensus splice mutation in the human dystrophin gene detected by a screening for intra-exonic deletions
F A Saad, L Vitiello, L Merlini, et al.
Neuromuscular Disorders : NMD
|
March 1, 1993
Dystrophin-positive myotubes in innervated muscle cultures from Duchenne and Becker muscular dystrophy patients
M Fanin, E P Hoffman, F A Saad, et al.
Human Genetics
|
May 1, 1990
Segregation analysis of 1885 DMD families: significant departure from the expected proportion of sporadic cases
G Barbujani, A Russo, G A Danieli, et al.
Biochemical and Biophysical Research Communications
|
November 5, 1999
Fine mapping and genomic structure of ACTN2, the human gene coding for the sarcomeric isoform of alpha-actinin-2, expressed in skeletal and cardiac muscle
N Tiso, M Majetti, F Stanchi, et al.
Annals of Human Genetics
|
March 16, 2007
Association between human polymorphic DNA markers and hypoxia adaptation in Sherpa detected by a preliminary genome scan
S Malacrida, Y Katsuyama, Y Droma, et al.
Human Genetics
|
May 1, 1993
Patterns of deletions of the dystrophin gene in different European populations
G A Danieli, F Mioni, C R Müller, et al.
Cytogenetics and Cell Genetics
|
January 1, 1997
Chromosomal localization of four MAPK signaling cascade genes: MEK1, MEK3, MEK4 and MEKK5
L Rampoldi, R Zimbello, S Bortoluzzi, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 96) with videos related to
Sort By:
Page
of 10
Muscle & Nerve
|
September 1, 1996
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?
M Fanin, M P Freda, L Vitiello, et al.
Nucleic Acids Research
|
October 11, 1994
Single base substitutions are detected by double strand conformation analysis
F A Saad, B Halliger, C R Müller, et al.
Neuroepidemiology
|
January 1, 1995
Frequency of duplication at 17p11.2 in families of northeast Italy with Charcot-Marie-Tooth disease type 1
M L Mostacciuolo, F Schiavon, C Angelini, et al.
Human Molecular Genetics
|
August 1, 1992
A 3' consensus splice mutation in the human dystrophin gene detected by a screening for intra-exonic deletions
F A Saad, L Vitiello, L Merlini, et al.
Neuromuscular Disorders : NMD
|
March 1, 1993
Dystrophin-positive myotubes in innervated muscle cultures from Duchenne and Becker muscular dystrophy patients
M Fanin, E P Hoffman, F A Saad, et al.
Human Genetics
|
May 1, 1990
Segregation analysis of 1885 DMD families: significant departure from the expected proportion of sporadic cases
G Barbujani, A Russo, G A Danieli, et al.
Biochemical and Biophysical Research Communications
|
November 5, 1999
Fine mapping and genomic structure of ACTN2, the human gene coding for the sarcomeric isoform of alpha-actinin-2, expressed in skeletal and cardiac muscle
N Tiso, M Majetti, F Stanchi, et al.
Annals of Human Genetics
|
March 16, 2007
Association between human polymorphic DNA markers and hypoxia adaptation in Sherpa detected by a preliminary genome scan
S Malacrida, Y Katsuyama, Y Droma, et al.
Human Genetics
|
May 1, 1993
Patterns of deletions of the dystrophin gene in different European populations
G A Danieli, F Mioni, C R Müller, et al.
Cytogenetics and Cell Genetics
|
January 1, 1997
Chromosomal localization of four MAPK signaling cascade genes: MEK1, MEK3, MEK4 and MEKK5
L Rampoldi, R Zimbello, S Bortoluzzi, et al.
Page
of 10