[HTML][HTML] Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function
GJ Bassell, ST Warren�- Neuron, 2008 - cell.com
Fragile X syndrome is the most common inherited form of cognitive deficiency in humans
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
GJ Bassell, ST Warren�- Neuron, 2008 - hero.epa.gov
Fragile X syndrome is the most common inherited form of cognitive deficiency in humans
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
[HTML][HTML] Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
GJ Bassell, ST Warren�- Neuron, 2008 - Elsevier
Fragile X syndrome is the most common inherited form of cognitive deficiency in humans
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function.
GJ Bassell, ST Warren�- Neuron, 2008 - europepmc.org
Fragile X syndrome is the most common inherited form of cognitive deficiency in humans
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function
GJ Bassell, ST Warren - 2008 - repository.escholarship.umassmed�…
Fragile X syndrome is the most common inherited form of cognitive deficiency in humans
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
GJ Bassell, ST Warren�- Neuron, 2008 - infona.pl
Fragile X syndrome is the most common inherited form of cognitive deficiency in humans
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
[CITATION][C] Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
GJ Bassell, ST Warren�- Neuron, 2008 - cir.nii.ac.jp
Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and
Function | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索�…
Function | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索�…
[PDF][PDF] Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
GJ Bassell, ST Warren�- Neuron, 2008 - Citeseer
Fragile X syndrome is the most common inherited form of cognitive deficiency in humans
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
[PDF][PDF] Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
GJ Bassell, ST Warren�- Neuron, 2008 - core.ac.uk
Fragile X syndrome is the most common inherited form of cognitive deficiency in humans
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function
GJ Bassell, ST Warren�- Neuron, 2008 - pubmed.ncbi.nlm.nih.gov
Fragile X syndrome is the most common inherited form of cognitive deficiency in humans
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion�…