Rare structural variation of synapse and neurotransmission genes in autism von Gai, X, Xie, H M, Perin, J C, Takahashi, N, Murphy, K, Wenocur, A S, D'arcy, M, O'Hara, R J, Goldmuntz, E, Grice, D E, Shaikh, T H, Hakonarson, H, Buxbaum, J D, Elia, J, White, P S

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Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome : genomic organization and deletion endpoint analysis von SHAIKH, T. H, KURAHASHI, H, EMANUEL, B. S, SAITTA, S. C, O'HARE, A. M, PING HU, ROE, B. A, DRISCOLL, D. A, MCDONALD-MCGINN, D. M, ZACKAI, E. H, BUDARF, M. L

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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes von Elia, J, Gai, X, Xie, H M, Perin, J C, Geiger, E, Glessner, J T, D'arcy, M, deBerardinis, R, Frackelton, E, Kim, C, Lantieri, F, Muganga, B M, Wang, L, Takeda, T, Rappaport, E F, Grant, S F A, Berrettini, W, Devoto, M, Shaikh, T H, Hakonarson, H, White, P S

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FTIR characterization and physicochemical evaluation of cottonseed oil von Shah, S. N.

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Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22) von KURAHASHI, H, SHAIKH, T. H, PING HU, ROE, B. A, EMANUEL, B. S, BUDARF, M. L

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African Origin of Human-Specific Polymorphic Alu Insertions von Batzer, Mark A., Stoneking, Mark, Alegria-Hartman, Michelle, Bazan, Hernan, Kass, David H., Shaikh, Tamim H., Novick, Gabriel E., Ioannou, Panayiotis A., Scheer, W. Douglas, Herrera, Rene J., Deininger, Prescott L.

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Tightly Clustered 11q23 and 22q11 Breakpoints Permit PCR-Based Detection of the Recurrent Constitutional t(11;22) von Kurahashi, Hiroki, Shaikh, Tamim H., Zackai, Elaine H., Celle, Livija, Driscoll, Deborah A., Budarf, Marcia L., Emanuel, Beverly S.

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Clustered 11q23 and 22q11 Breakpoints and 3:1 Meiotic Malsegregation in Multiple Unrelated t(11;22) Families von Shaikh, Tamim H., Budarf, Marcia L., Celle, Livija, Zackai, Elaine H., Emanuel, Beverly S.

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Segmental duplications: an 'expanding' role in genomic instability and disease von Emanuel, Beverly S., Shaikh, Tamim H.

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A 22q11.2 Deletion That Excludes UFD1L and CDC45L in a Patient with Conotruncal and Craniofacial Defects von Saitta, Sulagna C., McGrath, James M., Mensch, Holly, Shaikh, Tamim H., Zackai, Elaine H., Emanuel, Beverly S.

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Structure and variability of recently inserted alu family members von BDATZER, M. A, KILROY, G. E, RICHARD, P. E, SHAIKH, T. H, DESSELLE, T. D, HOPPENS, C. L, DEININGER, P. L

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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes von Elia, J, Gai, X, Xie, H M, Perin, J C, Geiger, E, Glessner, J T, D'arcy, M, Deberardinis, R, Frackelton, E, Kim, C, Lantieri, F, Muganga, B M, Wang, L, Takeda, T, Rappaport, E F, Grant, S F A, Berrettini, W, Devoto, M, Shaikh, T H, Hakonarson, H, White, P S

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Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: An update and literature review von Shaikh, Tamim H, Kurahashi, Hiroki, Emanuel, Beverly S

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Cis-acting influences on Alu RNA levels von Alemán, C, Roy-Engel, A M, Shaikh, T H, Deininger, P L

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Alu-mediated PCR artifacts and the constitutional t(11;22) breakpoint von KURAHASHI, Hiroki, SHAIKH, Tamim H, EMANUEL, Beverly S

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cDNAs derived from primary and small cytoplasmic Alu (scAlu) transcripts von Shaikh, Tamim H, Roy, Astrid M, Kim, Joomyeong, Batzer, Mark A, Deininger, Prescott L

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Identification of familial and de novo microduplications of 22q11.21–q11.23 distal to the 22q11.21 microdeletion syndrome region von Coppinger, Justine, McDonald-McGinn, Donna, Zackai, Elaine, Shane, Kate, Atkin, Joan F., Asamoah, Alexander, Leland, Robert, Weaver, David D., Lansky-Shafer, Susan, Schmidt, Karen, Feldman, Heidi, Cohen, William, Phalin, Judy, Powell, Berkley, Ballif, Blake C., Theisen, Aaron, Geiger, Elizabeth, Haldeman-Englert, Chad, Shaikh, Tamim H., Saitta, Sulagna, Bejjani, Bassem A., Shaffer, Lisa G.

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Dispersion and insertion polymorphism in two small subfamilies of recently amplified human Alu repeats von Batzer, M A, Rubin, C M, Hellmann-Blumberg, U, Alegria-Hartman, M, Leeflang, E P, Stern, J D, Bazan, H A, Shaikh, T H, Deininger, P L, Schmid, C W

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Oligonucleotide arrays for high-resolution analysis of copy number alteration in mental retardation/multiple congenital anomalies von Shaikh, Tamim H

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The role and amplification of the HS Alu subfamily founder gene von Shaikh, T H, Deininger, P L

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