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T H Shaikh

Showing results (11-20 of 19) with videos related to

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Biotechniques|March 1, 1992
Large-scale subcloning of bacteriophage lambda ZAP clonesM A Batzer, H A Bazan, J Kim, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 2, 1999
Characterization of CDC45L: a gene in the 22q11.2 deletion region expressed during murine and human developmentT H Shaikh, S Gottlieb, B Sellinger, et al.
Nucleic Acids Research|December 11, 1990
Structure and variability of recently inserted Alu family membersM A Batzer, G E Kilroy, P E Richard, et al.
Gene|October 3, 1995
Sequence diversity and chromosomal distribution of "young" Alu repeatsS S Arcot, T H Shaikh, J Kim, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 6, 1994
African origin of human-specific polymorphic Alu insertionsM A Batzer, M Stoneking, M Alegria-Hartman, et al.
Journal of Molecular Biology|March 31, 1995
Dispersion and insertion polymorphism in two small subfamilies of recently amplified human Alu repeatsM A Batzer, C M Rubin, U Hellmann-Blumberg, et al.
Human Molecular Genetics|March 4, 2000
Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysisT H Shaikh, H Kurahashi, S C Saitta, et al.
Molecular Psychiatry|March 2, 2011
Rare structural variation of synapse and neurotransmission genes in autismX Gai, H M Xie, J C Perin, et al.
Molecular Psychiatry|June 24, 2009
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genesJ Elia, X Gai, H M Xie, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Biotechniques|March 1, 1992
Large-scale subcloning of bacteriophage lambda ZAP clonesM A Batzer, H A Bazan, J Kim, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 2, 1999
Characterization of CDC45L: a gene in the 22q11.2 deletion region expressed during murine and human developmentT H Shaikh, S Gottlieb, B Sellinger, et al.
Nucleic Acids Research|December 11, 1990
Structure and variability of recently inserted Alu family membersM A Batzer, G E Kilroy, P E Richard, et al.
Gene|October 3, 1995
Sequence diversity and chromosomal distribution of "young" Alu repeatsS S Arcot, T H Shaikh, J Kim, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 6, 1994
African origin of human-specific polymorphic Alu insertionsM A Batzer, M Stoneking, M Alegria-Hartman, et al.
Journal of Molecular Biology|March 31, 1995
Dispersion and insertion polymorphism in two small subfamilies of recently amplified human Alu repeatsM A Batzer, C M Rubin, U Hellmann-Blumberg, et al.
Human Molecular Genetics|March 4, 2000
Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysisT H Shaikh, H Kurahashi, S C Saitta, et al.
Molecular Psychiatry|March 2, 2011
Rare structural variation of synapse and neurotransmission genes in autismX Gai, H M Xie, J C Perin, et al.
Molecular Psychiatry|June 24, 2009
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genesJ Elia, X Gai, H M Xie, et al.
Pageof 2