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Pediatric Neurology
|
January 1, 1993
Progressive juvenile segmental spinal muscular atrophy
G T Liu, L A Specht
Pediatric Neurology
|
September 1, 1991
Childhood onset oculopharyngeal muscular dystrophy
D Lacomis, W J Kupsky, K K Kuban, et al.
Brain Research
|
August 10, 1981
Fine structure of the nigrostriatal anlage in fetal rat brain by immunocytochemical localization of tyrosine hydroxylase
L A Specht, V M Pickel, T H Joh, et al.
Nature Genetics
|
May 1, 1994
Mapping a gene for congenital fibrosis of the extraocular muscles to the centromeric region of chromosome 12
E C Engle, L M Kunkel, L A Specht, et al.
The Journal of Comparative Neurology
|
June 20, 1981
Light-microscopic immunocytochemical localization of tyrosine hydroxylase in prenatal rat brain. I. Early ontogeny
L A Specht, V M Pickel, T H Joh, et al.
The Journal of Comparative Neurology
|
June 20, 1981
Light-microscopic immunocytochemical localization of tyrosine hydroxylase in prenatal rat brain. II. Late ontogeny
L A Specht, V M Pickel, T H Joh, et al.
Pediatric Neurology
|
November 1, 1992
Prediction of dystrophin phenotype by DNA analysis in Duchenne/Becker muscular dystrophy
L A Specht, A H Beggs, B Korf, et al.
Journal of Child Neurology
|
July 1, 1996
Congenital muscular dystrophy associated with merosin deficiency
K N North, L A Specht, R K Sethi, et al.
The Journal of Comparative Neurology
|
November 15, 1980
Immunocytochemical localization of tyrosine hydroxylase in the human fetal nervous system
V M Pickel, L A Specht, K K Sumal, et al.
American Journal of Medical Genetics
|
January 24, 1998
Increase in fetal breech presentation in female carriers of Duchenne muscular dystrophy
O Geifman-Holtzman, I M Bernstein, E L Capeless, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
Pediatric Neurology
|
January 1, 1993
Progressive juvenile segmental spinal muscular atrophy
G T Liu, L A Specht
Pediatric Neurology
|
September 1, 1991
Childhood onset oculopharyngeal muscular dystrophy
D Lacomis, W J Kupsky, K K Kuban, et al.
Brain Research
|
August 10, 1981
Fine structure of the nigrostriatal anlage in fetal rat brain by immunocytochemical localization of tyrosine hydroxylase
L A Specht, V M Pickel, T H Joh, et al.
Nature Genetics
|
May 1, 1994
Mapping a gene for congenital fibrosis of the extraocular muscles to the centromeric region of chromosome 12
E C Engle, L M Kunkel, L A Specht, et al.
The Journal of Comparative Neurology
|
June 20, 1981
Light-microscopic immunocytochemical localization of tyrosine hydroxylase in prenatal rat brain. I. Early ontogeny
L A Specht, V M Pickel, T H Joh, et al.
The Journal of Comparative Neurology
|
June 20, 1981
Light-microscopic immunocytochemical localization of tyrosine hydroxylase in prenatal rat brain. II. Late ontogeny
L A Specht, V M Pickel, T H Joh, et al.
Pediatric Neurology
|
November 1, 1992
Prediction of dystrophin phenotype by DNA analysis in Duchenne/Becker muscular dystrophy
L A Specht, A H Beggs, B Korf, et al.
Journal of Child Neurology
|
July 1, 1996
Congenital muscular dystrophy associated with merosin deficiency
K N North, L A Specht, R K Sethi, et al.
The Journal of Comparative Neurology
|
November 15, 1980
Immunocytochemical localization of tyrosine hydroxylase in the human fetal nervous system
V M Pickel, L A Specht, K K Sumal, et al.
American Journal of Medical Genetics
|
January 24, 1998
Increase in fetal breech presentation in female carriers of Duchenne muscular dystrophy
O Geifman-Holtzman, I M Bernstein, E L Capeless, et al.
Page
of 2