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L A Specht

Showing results (1-10 of 13) with videos related to

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Pediatric Neurology|January 1, 1993
Progressive juvenile segmental spinal muscular atrophyG T Liu, L A Specht
Pediatric Neurology|September 1, 1991
Childhood onset oculopharyngeal muscular dystrophyD 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 hydroxylaseL 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 12E 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 ontogenyL 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 ontogenyL 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 dystrophyL A Specht, A H Beggs, B Korf, et al.
Journal of Child Neurology|July 1, 1996
Congenital muscular dystrophy associated with merosin deficiencyK 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 systemV 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 dystrophyO Geifman-Holtzman, I M Bernstein, E L Capeless, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Pediatric Neurology|January 1, 1993
Progressive juvenile segmental spinal muscular atrophyG T Liu, L A Specht
Pediatric Neurology|September 1, 1991
Childhood onset oculopharyngeal muscular dystrophyD 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 hydroxylaseL 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 12E 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 ontogenyL 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 ontogenyL 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 dystrophyL A Specht, A H Beggs, B Korf, et al.
Journal of Child Neurology|July 1, 1996
Congenital muscular dystrophy associated with merosin deficiencyK 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 systemV 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 dystrophyO Geifman-Holtzman, I M Bernstein, E L Capeless, et al.
Pageof 2