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European Journal of Human Genetics : EJHG
|
April 10, 1999
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex
M Vainzof, E S Moreira, G Ferraz, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1984
Thymosin increases production of T-cell growth factor by normal human peripheral blood lymphocytes
M M Zatz, J Oliver, C Samuels, et al.
Human Molecular Genetics
|
March 1, 1995
Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?
M Zatz, M R Passos-Bueno, A Cerqueira, et al.
Human Molecular Genetics
|
August 15, 2000
Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome)
A L Sertié, V Sossi, A A Camargo, et al.
Muscle & Nerve
|
May 8, 2002
Lack of the C-terminal domain of nebulin in a patient with nemaline myopathy
J Gurgel-Giannetti, M-L Bang, U Reed, et al.
Journal of Medical Genetics
|
December 1, 1998
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies
E S Moreira, M Vainzof, S K Marie, et al.
American Journal of Medical Genetics
|
May 30, 1998
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females
M Zatz, S K Marie, A Cerqueira, et al.
American Journal of Medical Genetics
|
October 1, 1986
Duchenne muscular dystrophy in a girl with a 45,X/46,XX/47,XXX chromosome constitution
E R Bortolini, D M da Silva, R S Chequer, et al.
American Journal of Medical Genetics
|
August 26, 1998
Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases
M Zatz, D Sumita, S Campiotto, et al.
Psychiatry Research
|
August 1, 1982
CT measures of cerebrospinal fluid volume in alcoholics and normal volunteers
T L Jernigan, L M Zatz, A J Ahumada, et al.
Page
of 26
Search research articles
Search
Showing results (151-160 of 252) with videos related to
Sort By:
Page
of 26
European Journal of Human Genetics : EJHG
|
April 10, 1999
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex
M Vainzof, E S Moreira, G Ferraz, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1984
Thymosin increases production of T-cell growth factor by normal human peripheral blood lymphocytes
M M Zatz, J Oliver, C Samuels, et al.
Human Molecular Genetics
|
March 1, 1995
Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?
M Zatz, M R Passos-Bueno, A Cerqueira, et al.
Human Molecular Genetics
|
August 15, 2000
Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome)
A L Sertié, V Sossi, A A Camargo, et al.
Muscle & Nerve
|
May 8, 2002
Lack of the C-terminal domain of nebulin in a patient with nemaline myopathy
J Gurgel-Giannetti, M-L Bang, U Reed, et al.
Journal of Medical Genetics
|
December 1, 1998
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies
E S Moreira, M Vainzof, S K Marie, et al.
American Journal of Medical Genetics
|
May 30, 1998
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females
M Zatz, S K Marie, A Cerqueira, et al.
American Journal of Medical Genetics
|
October 1, 1986
Duchenne muscular dystrophy in a girl with a 45,X/46,XX/47,XXX chromosome constitution
E R Bortolini, D M da Silva, R S Chequer, et al.
American Journal of Medical Genetics
|
August 26, 1998
Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases
M Zatz, D Sumita, S Campiotto, et al.
Psychiatry Research
|
August 1, 1982
CT measures of cerebrospinal fluid volume in alcoholics and normal volunteers
T L Jernigan, L M Zatz, A J Ahumada, et al.
Page
of 26