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C A Walsh

Showing results (81-90 of 128) with videos related to

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Neuron|August 12, 2000
Reelin binds alpha3beta1 integrin and inhibits neuronal migrationL Dulabon, E C Olson, M G Taglienti, et al.
Neurology|May 29, 2003
A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21A Rajab, G H Mochida, A Hill, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 1, 1992
Evidence for P2-purinoceptors on human osteoblast-like cellsC Schöfl, K S Cuthbertson, C A Walsh, et al.
Neurology|May 5, 1998
X-linked female band heterotopia-male lissencephaly syndromeM J Berg, G Schifitto, J M Powers, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 1, 1995
Expression and secretion of parathyroid hormone-related protein by human bone-derived cells in vitro: effects of glucocorticoidsC A Walsh, M A Birch, W D Fraser, et al.
Journal of Neurology|February 1, 2000
Studies of the candidate genes in X-linked congenital cerebellar hypoplasiaS N Illarioshkin, K M Allen, J G Gleeson, et al.
Optics Letters|October 2, 2009
Subsecond grating growth in a photorefractive polymerS M Silence, C A Walsh, J C Scott, et al.
Nature Genetics|September 10, 1998
PAK3 mutation in nonsyndromic X-linked mental retardationK M Allen, J G Gleeson, S Bagrodia, et al.
Nature Genetics|September 6, 2000
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutationsS E Hong, Y Y Shugart, D T Huang, et al.
Neurology|January 13, 2006
A familial syndrome of unilateral polymicrogyria affecting the right hemisphereB S Chang, K A Apse, R Caraballo, et al.
Pageof 13

Showing results (81-90 of 128) with videos related to

Sort By:
Pageof 13
Neuron|August 12, 2000
Reelin binds alpha3beta1 integrin and inhibits neuronal migrationL Dulabon, E C Olson, M G Taglienti, et al.
Neurology|May 29, 2003
A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21A Rajab, G H Mochida, A Hill, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 1, 1992
Evidence for P2-purinoceptors on human osteoblast-like cellsC Schöfl, K S Cuthbertson, C A Walsh, et al.
Neurology|May 5, 1998
X-linked female band heterotopia-male lissencephaly syndromeM J Berg, G Schifitto, J M Powers, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 1, 1995
Expression and secretion of parathyroid hormone-related protein by human bone-derived cells in vitro: effects of glucocorticoidsC A Walsh, M A Birch, W D Fraser, et al.
Journal of Neurology|February 1, 2000
Studies of the candidate genes in X-linked congenital cerebellar hypoplasiaS N Illarioshkin, K M Allen, J G Gleeson, et al.
Optics Letters|October 2, 2009
Subsecond grating growth in a photorefractive polymerS M Silence, C A Walsh, J C Scott, et al.
Nature Genetics|September 10, 1998
PAK3 mutation in nonsyndromic X-linked mental retardationK M Allen, J G Gleeson, S Bagrodia, et al.
Nature Genetics|September 6, 2000
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutationsS E Hong, Y Y Shugart, D T Huang, et al.
Neurology|January 13, 2006
A familial syndrome of unilateral polymicrogyria affecting the right hemisphereB S Chang, K A Apse, R Caraballo, et al.
Pageof 13