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J G Gleeson

Showing results (31-40 of 36) with videos related to

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Clinical Genetics|June 21, 2008
RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disordersF Brancati, L Travaglini, D Zablocka, et al.
Cell|March 7, 1998
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling proteinJ G Gleeson, K M Allen, J W Fox, et al.
Annals of Neurology|February 9, 2000
Genetic and neuroradiological heterogeneity of double cortex syndromeJ G Gleeson, R F Luo, P E Grant, et al.
Neurology|January 26, 2011
Distinguishing 3 classes of corpus callosal abnormalities in consanguineous familiesR M Hanna, S E Marsh, D Swistun, et al.
Human Molecular Genetics|April 1, 1997
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brainM E Ross, K M Allen, A K Srivastava, et al.
Annals of Neurology|February 16, 1999
Characterization of mutations in the gene doublecortin in patients with double cortex syndromeJ G Gleeson, S R Minnerath, J W Fox, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Clinical Genetics|June 21, 2008
RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disordersF Brancati, L Travaglini, D Zablocka, et al.
Cell|March 7, 1998
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling proteinJ G Gleeson, K M Allen, J W Fox, et al.
Annals of Neurology|February 9, 2000
Genetic and neuroradiological heterogeneity of double cortex syndromeJ G Gleeson, R F Luo, P E Grant, et al.
Neurology|January 26, 2011
Distinguishing 3 classes of corpus callosal abnormalities in consanguineous familiesR M Hanna, S E Marsh, D Swistun, et al.
Human Molecular Genetics|April 1, 1997
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brainM E Ross, K M Allen, A K Srivastava, et al.
Annals of Neurology|February 16, 1999
Characterization of mutations in the gene doublecortin in patients with double cortex syndromeJ G Gleeson, S R Minnerath, J W Fox, et al.
Pageof 4