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T H Shaikh

Showing results (1-10 of 19) with videos related to

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Nature Reviews. Genetics|October 5, 2001
Segmental duplications: an 'expanding' role in genomic instability and diseaseB S Emanuel, T H Shaikh
Journal of Molecular Evolution|January 1, 1996
The role and amplification of the HS Alu subfamily founder geneT H Shaikh, P L Deininger
Human Molecular Genetics|November 7, 2000
Alu-mediated PCR artifacts and the constitutional t(11;22) breakpointH Kurahashi, T H Shaikh, B S Emanuel
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: an update and literature reviewT H Shaikh, H Kurahashi, B S Emanuel
Nucleic Acids Research|November 30, 2000
Cis-acting influences on Alu RNA levelsC Alemán, A M Roy-Engel, T H Shaikh, et al.
Journal of Molecular Biology|August 15, 1997
cDNAs derived from primary and small cytoplasmic Alu (scAlu) transcriptsT H Shaikh, A M Roy, J Kim, et al.
American Journal of Human Genetics|December 1, 1999
Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) familiesT H Shaikh, M L Budarf, L Celle, et al.
Human Molecular Genetics|June 22, 2000
Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22)H Kurahashi, T H Shaikh, P Hu, et al.
American Journal of Human Genetics|July 27, 1999
A 22q11.2 deletion that excludes UFD1L and CDC45L in a patient with conotruncal and craniofacial defectsS C Saitta, J M McGrath, H Mensch, et al.
American Journal of Human Genetics|July 25, 2000
Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22)H Kurahashi, T H Shaikh, E H Zackai, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Nature Reviews. Genetics|October 5, 2001
Segmental duplications: an 'expanding' role in genomic instability and diseaseB S Emanuel, T H Shaikh
Journal of Molecular Evolution|January 1, 1996
The role and amplification of the HS Alu subfamily founder geneT H Shaikh, P L Deininger
Human Molecular Genetics|November 7, 2000
Alu-mediated PCR artifacts and the constitutional t(11;22) breakpointH Kurahashi, T H Shaikh, B S Emanuel
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: an update and literature reviewT H Shaikh, H Kurahashi, B S Emanuel
Nucleic Acids Research|November 30, 2000
Cis-acting influences on Alu RNA levelsC Alemán, A M Roy-Engel, T H Shaikh, et al.
Journal of Molecular Biology|August 15, 1997
cDNAs derived from primary and small cytoplasmic Alu (scAlu) transcriptsT H Shaikh, A M Roy, J Kim, et al.
American Journal of Human Genetics|December 1, 1999
Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) familiesT H Shaikh, M L Budarf, L Celle, et al.
Human Molecular Genetics|June 22, 2000
Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22)H Kurahashi, T H Shaikh, P Hu, et al.
American Journal of Human Genetics|July 27, 1999
A 22q11.2 deletion that excludes UFD1L and CDC45L in a patient with conotruncal and craniofacial defectsS C Saitta, J M McGrath, H Mensch, et al.
American Journal of Human Genetics|July 25, 2000
Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22)H Kurahashi, T H Shaikh, E H Zackai, et al.
Pageof 2