3q29 interstitial microduplication: A new syndrome in a three-generation family von Lisi, Emily C., Hamosh, Ada, Doheny, Kimberly F., Squibb, Elizabeth, Jackson, Barbara, Galczynski, Rebecca, Thomas, George H., Batista, Denise A.S.

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Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor von Loeys, Bart L, Schwarze, Ulrike, Holm, Tammy, Callewaert, Bert L, Thomas, George H, Pannu, Hariyadarshi, De Backer, Julie F, Oswald, Gretchen L, Symoens, Sofie, Manouvrier, Sylvie, Roberts, Amy E, Faravelli, Francesca, Greco, M. Alba, Pyeritz, Reed E, Milewicz, Dianna M, Coucke, Paul J, Cameron, Duke E, Braverman, Alan C, Byers, Peter H, De Paepe, Anne M, Dietz, Harry C

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Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan von Ting, Jason C, Ye, Ying, Thomas, George H, Ruczinski, Ingo, Pevsner, Jonathan

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Congenital T Cell Deficiency in a Patient with CHARGE Syndrome von Hoover-Fong, Julie, MD, PhD, Savage, William J., MD, Lisi, Emily, MS, Winkelstein, Jerry, MD, Thomas, George H., PhD, Hoefsloot, Lies H., PhD, Loeb, David M., MD, PhD

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Recurrent 10q22-q23 Deletions: A Genomic Disorder on 10q Associated with Cognitive and Behavioral Abnormalities von Balciuniene, Jorune, Feng, Ningping, Iyadurai, Kelly, Hirsch, Betsy, Charnas, Lawrence, Bill, Brent R., Easterday, Mathew C., Staaf, Johan, Oseth, LeAnn, Czapansky-Beilman, Desiree, Avramopoulos, Dimitri, Thomas, George H., Borg, Åke, Valle, David, Schimmenti, Lisa A., Selleck, Scott B.

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Genomic analysis of partial 21q monosomies with variable phenotypes von Roberson, Elisha D O, Wohler, Elizabeth Squibb, Hoover-Fong, Julie E, Lisi, Emily, Stevens, Eric L, Thomas, George H, Leonard, Jay, Hamosh, Ada, Pevsner, Jonathan

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Optical determination of Cr(VI) using regenerable, functionalized sol–gel monoliths von Carrington, Nathan A., Thomas, George H., Rodman, D. Lynn, Beach, David B., Xue, Zi-Ling

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Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: Evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function von Miller, Nathaniel D., Nance, Melonie A., Wohler, Elizabeth S., Hoover-Fong, Julie E., Lisi, Emily, Thomas, George H., Pevsner, Jonathan

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Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio von Ting, Jason C, Roberson, Elisha D.O, Miller, Nathaniel D, Lysholm-Bernacchi, Alana, Stephan, Dietrich A, Capone, George T, Ruczinski, Ingo, Thomas, George H, Pevsner, Jonathan

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Growth of epitaxial films of sodium potassium tantalate and niobate on single-crystal lanthanum aluminate [100] substrates von Thomas, George H., Specht, Eliot D., Larese, John Z., Xue, Ziling B., Beach, David B.

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A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9 von Boyadjiev, Simeon A., South, Sarah T., Radford, Cristi L., Patel, Ankita, Zhang, George, Hur, David J., Thomas, George H., Gearhart, John P., Stetten, Gail

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Molecular cytogenetic analysis of a de novo interstitial deletion of chromosome 10q (q25.3q26.13) in a male child with ambiguous genitalia: Evidence for a new critical region for g... von Mardo, Veronica, Squibb, Elizabeth E., Braverman, Nancy, Hoover-Fong, Julie E., Migeon, Claude, Batista, Denise A.S., Thomas, George H.

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Cryptic subtelomeric translocations in the 22q13 deletion syndrome von Praphanphoj, Verayuth, Goodman, Barbara K, Thomas, George H, Raymond, Gerald V

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Characterization of the human gene encoding α-aminoadipate aminotransferase (AADAT) von Goh, Denise L.M, Patel, Ankita, Thomas, George H, Salomons, Gajja S, Schor, Danielle S.M, Jakobs, Cornelis, Geraghty, Michael T

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Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus: A Cause of Postpartum Coma von Arn, Pamela Hawks, Hauser, Elizabeth R, Thomas, George H, Herman, Gail, Hess, David, Brusilow, Saul W

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Merkel Cell Carcinoma in a Male Breast: A Case Report von Alzaraa, Ahmed, Thomas, George D.H., Vodovnik, Alexander, Modgill, Vijay K

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Genomic analysis of partial 21p monosomies with variable phenotypes von ROBERSON, Elisha Do, SQUIBB WOHLER, Elizabeth, HOOVER-FONG, Julie E, LISI, Emily, STEVENS, Eric L, THOMAS, George H, LEONARD, Jay, HAMOSH, Ada, PEVSNER, Jonathan

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Two Anonymous DNA Segments Distinguish the Wilms' Tumor and Aniridia Loci von Davis, Lisa M., Stallard, Richard, Thomas, George H., Couillin, Philippe, Junien, Claudine, Nowak, Norma J., Shows, Thomas B.

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Hydroxyurea: Effects on Hemoglobin F Production in Patients With Sickle Cell Anemia von Charache, Samuel, Dover, George J., Moore, Richard D., Eckert, S., Ballas, Samir K., Koshy, Mabel, Milner, Paul F.A., Orringer, Eugene P., Phillips, George, Platt, Orah S., Thomas, George H.

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Alan Tawse Edwards von Thomas, George D H

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