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Human Genetics
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October 30, 1999
Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy?
M D'Alessandro, I Naom, A Ferlini, et al.
Tissue Antigens
|
November 1, 1996
A new allelic variant of HLA-DRB1*1101 (DRB1*11013) segregating in a Sardinian family
M R Murru, G Costa, R Murru, et al.
American Journal of Human Genetics
|
July 31, 1998
A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathy
A Ferlini, N Galié, L Merlini, et al.
Brain : a Journal of Neurology
|
May 13, 1998
Abnormal merosin in adults. A new form of late onset muscular dystrophy not linked to chromosome 6q2
K Bushby, L V Anderson, C Pollitt, et al.
Neurology
|
May 22, 1998
Charcot-Marie-Tooth disease type 2 associated with mutation of the myelin protein zero gene
M G Marrosu, S Vaccargiu, G Marrosu, et al.
Circulation
|
February 9, 2000
Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement
G L Brodsky, F Muntoni, S Miocic, et al.
Neurology
|
February 1, 1997
A novel point mutation in the peripheral myelin protein 22 (PMP22) gene associated with Charcot-Marie-Tooth disease type 1A
M G Marrosu, S Vaccargiu, G Marrosu, et al.
Neuroscience Letters
|
April 11, 1986
Responsiveness to 'autoreceptor' doses of apomorphine inversely correlated with the firing rate of dopaminergic A9 neurons: action of baclofen
G Mereu, F Muntoni, P Calabresi, et al.
Neuromuscular Disorders : NMD
|
June 19, 2001
Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect?
J Philpot, S Counsell, G Bydder, et al.
Clinical Genetics
|
May 1, 1993
Germinal mosaicism in a Duchenne muscular dystrophy family: implications for genetic counselling
M A Melis, M Cau, R Congiu, et al.
Page
of 28
Search research articles
Search
Showing results (71-80 of 275) with videos related to
Sort By:
Page
of 28
Human Genetics
|
October 30, 1999
Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy?
M D'Alessandro, I Naom, A Ferlini, et al.
Tissue Antigens
|
November 1, 1996
A new allelic variant of HLA-DRB1*1101 (DRB1*11013) segregating in a Sardinian family
M R Murru, G Costa, R Murru, et al.
American Journal of Human Genetics
|
July 31, 1998
A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathy
A Ferlini, N Galié, L Merlini, et al.
Brain : a Journal of Neurology
|
May 13, 1998
Abnormal merosin in adults. A new form of late onset muscular dystrophy not linked to chromosome 6q2
K Bushby, L V Anderson, C Pollitt, et al.
Neurology
|
May 22, 1998
Charcot-Marie-Tooth disease type 2 associated with mutation of the myelin protein zero gene
M G Marrosu, S Vaccargiu, G Marrosu, et al.
Circulation
|
February 9, 2000
Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement
G L Brodsky, F Muntoni, S Miocic, et al.
Neurology
|
February 1, 1997
A novel point mutation in the peripheral myelin protein 22 (PMP22) gene associated with Charcot-Marie-Tooth disease type 1A
M G Marrosu, S Vaccargiu, G Marrosu, et al.
Neuroscience Letters
|
April 11, 1986
Responsiveness to 'autoreceptor' doses of apomorphine inversely correlated with the firing rate of dopaminergic A9 neurons: action of baclofen
G Mereu, F Muntoni, P Calabresi, et al.
Neuromuscular Disorders : NMD
|
June 19, 2001
Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect?
J Philpot, S Counsell, G Bydder, et al.
Clinical Genetics
|
May 1, 1993
Germinal mosaicism in a Duchenne muscular dystrophy family: implications for genetic counselling
M A Melis, M Cau, R Congiu, et al.
Page
of 28