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R Sean Hill

Showing results (1-10 of 39) with videos related to

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American Journal of Medical Genetics. Part A|May 12, 2005
EMX2-independent familial schizencephaly: clinical and genetic analysesIan Tietjen, Füsun Erdogan, Sophie Currier, et al.
American Journal of Medical Genetics. Part A|July 3, 2007
A 2-Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndromeAnthony D Hill, Bernard S Chang, R Sean Hill, et al.
American Journal of Human Genetics|December 17, 2009
A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephalyGaneshwaran H Mochida, Muhammad Mahajnah, Anthony D Hill, et al.
Science (New York, N.Y.)|April 21, 2007
Comment on "Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens"Fuli Yu, R Sean Hill, Stephen F Schaffner, et al.
Annals of Neurology|April 28, 2006
Impaired proliferation and migration in human Miller-Dieker neural precursorsVolney L Sheen, Russell J Ferland, Megan Harney, et al.
Nature Genetics|December 3, 2003
Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortexVolney L Sheen, Vijay S Ganesh, Meral Topcu, et al.
Plos Genetics|April 19, 2012
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autismMaria H Chahrour, Timothy W Yu, Elaine T Lim, et al.
Nature Genetics|August 24, 2004
Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndromeRussell J Ferland, Wafaa Eyaid, Randall V Collura, et al.
Human Mutation|May 12, 2017
Deficient activity of alanyl-tRNA synthetase underlies an autosomal recessive syndrome of progressive microcephaly, hypomyelination, and epileptic encephalopathyTojo Nakayama, Jiang Wu, Patricia Galvin-Parton, et al.
Annals of Neurology|May 4, 2010
Developmental and degenerative features in a complicated spastic paraplegiaM Chiara Manzini, Anna Rajab, Thomas M Maynard, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics. Part A|May 12, 2005
EMX2-independent familial schizencephaly: clinical and genetic analysesIan Tietjen, Füsun Erdogan, Sophie Currier, et al.
American Journal of Medical Genetics. Part A|July 3, 2007
A 2-Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndromeAnthony D Hill, Bernard S Chang, R Sean Hill, et al.
American Journal of Human Genetics|December 17, 2009
A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephalyGaneshwaran H Mochida, Muhammad Mahajnah, Anthony D Hill, et al.
Science (New York, N.Y.)|April 21, 2007
Comment on "Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens"Fuli Yu, R Sean Hill, Stephen F Schaffner, et al.
Annals of Neurology|April 28, 2006
Impaired proliferation and migration in human Miller-Dieker neural precursorsVolney L Sheen, Russell J Ferland, Megan Harney, et al.
Nature Genetics|December 3, 2003
Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortexVolney L Sheen, Vijay S Ganesh, Meral Topcu, et al.
Plos Genetics|April 19, 2012
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autismMaria H Chahrour, Timothy W Yu, Elaine T Lim, et al.
Nature Genetics|August 24, 2004
Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndromeRussell J Ferland, Wafaa Eyaid, Randall V Collura, et al.
Human Mutation|May 12, 2017
Deficient activity of alanyl-tRNA synthetase underlies an autosomal recessive syndrome of progressive microcephaly, hypomyelination, and epileptic encephalopathyTojo Nakayama, Jiang Wu, Patricia Galvin-Parton, et al.
Annals of Neurology|May 4, 2010
Developmental and degenerative features in a complicated spastic paraplegiaM Chiara Manzini, Anna Rajab, Thomas M Maynard, et al.
Pageof 4