Genomic imbalances associated with müllerian aplasia von Cheroki, C, Krepischi-Santos, A C V, Szuhai, K, Brenner, V, Kim, C A E, Otto, P A, Rosenberg, C

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Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents von Rosenberg, C, Knijnenburg, J, Bakker, E, Vianna-Morgante, A M, Sloos, W, Otto, P A, Kriek, M, Hansson, K, Krepischi-Santos, A C V, Fiegler, H, Carter, N P, Bijlsma, E K, van Haeringen, A, Szuhai, K, Tanke, H J

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Chromosome imbalances in syndromic hearing loss von Catelani, ALPM, Krepischi, ACV, Kim, CA, Kok, F, Otto, PA, Auricchio, MTBM, Mazzeu, JF, Uehara, DT, Costa, SS, Knijnenburg, J, Tabith Jr, A, Vianna-Morgante, AM, Mingroni-Netto, RC, Rosenberg, C

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The short variant of the polymorphism within the promoter region of the serotonin transporter gene is a risk factor for late onset Alzheimer's disease von Oliveira, J R M, Gallindo, R M, Maia, L G S, Brito-Marques, P R, Otto, P A, Passos-Bueno, M R, Jr, MA Morais, Zatz, M

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A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21 von Lezirovitz, K, Braga, MCC, Thiele-Aguiar, RS, Auricchio, MTBM, Pearson, PL, Otto, PA, Mingroni-Netto, RC

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Evidence that BCL3 plays a role in the etiology of nonsyndromic oral clefts in Brazilian families von Gaspar, D.A., Matioli, S.R., Pavanello, R.C., Araújo, B.C., André, M., Steman, S., Otto, P.A., Passos-Bueno, M.R.

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Correspondence regarding Ballana et al., “Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment” von Abreu-Silva, R.S., Batissoco, A.C., Lezirovitz, K., Romanos, J., Rincon, D., Auricchio, M.T.B.M., Otto, P.A., Mingroni-Netto, R.C.

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Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations von Krepischi-Santos, A.C.V., Vianna-Morgante, A.M., Jehee, F.S., Passos-Bueno, M.R., Knijnenburg, J., Szuhai, K., Sloos, W., Mazzeu, J.F., Kok, F., Cheroki, C., Otto, P.A., Mingroni-Netto, R.C., Varela, M., Koiffmann, C., Kim, C.A., Bertola, D.R., Pearson, P.L., Rosenberg, C.

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Release characteristics of cardiac biomarkers and ischemia-modified albumin as measured by the albumin cobalt-binding test after a marathon race von APPLE, Fred S, QUIST, Heidi E, OTTO, Angela P, MATHEWS, Wendy E, MURAKAMI, Maryann M

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Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in Brazilian patients affected by bipolar disorder and schizophreni... von de Oliveira, João R. Mendes, Otto, Paulo A., Vallada, Homero, Lauriano, Valéria, Elkis, Helio, Lafer, Beny, Vasquez, Luciana, Gentil, Valentim, Passos-Bueno, M. Rita, Zatz, Mayana

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Constitutional Haploinsufficiency of Tumor Suppressor Genes in Mentally Retarded Patients With Microdeletions in 17p13.1 von Krepischi-Santos, A.C.V., Rajan, D., Temple, I.K., Shrubb, V., Crolla, J.A., Huang, S., Beal, S., Otto, P.A., Carter, N.P., Vianna-Morgante, A.M., Rosenberg, C.

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Red to blue upconversion in Tm-doped sol–gel silicate glasses von Otto, Allen P, Brewer, Karen S, Silversmith, Ann J

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The Maintenance of Sex, Clonal Dynamics, and Host‐Parasite Coevolution in a Mixed Population of Sexual and Asexual Snails von Jokela, Jukka, Dybdahl, Mark F., Lively, Curtis M.

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Analysis of the serotonin transporter polymorphism (5-HTTLPR) in Brazilian patients affected by dysthymia, major depression and bipolar disorder von Oliveira, J R, Carvalho, D R, Pontual, D, Gallindo, R M, Sougey, E B, Gentil, V, Lafer, B, Maia, L G, Morais, Jr, M A, Matioli, S, Vallada, H, Moreno, R A, Nishimura, A, Otto, P A, Passos-Bueno, M R, Zatz, M

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Exploring the Effect of Sex on Empirical Fitness Landscapes von de Visser, J. Arjan G. M., Park, Su‐Chan, Krug, Joachim

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Replication timing of homologous alpha-satellite DNA in Roberts syndrome von Barbosa, A C, Otto, P A, Vianna-Morgante, A M

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No evidence of association between the D10S1423 locus and Alzheimer disease in Brazilian patients von Nishimura, A L, Oliveira, J R, Otto, P A, Matioli, S R, Brito-Marques, P R, Bahia, V S, Nitrini, R, Zatz, M

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Rheumatic fever and the HLA complex : a cosegregation study von GERBASE-DELIMA, M, SCALA, L. C. N, TEMIN, J, SANTOS, D. V, OTTO, P. A

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An Illustrative Case of Neurofibromatosis Type 1 and NF1 Microdeletion von Praxedes, L.A., Pereira, F.M., Mazzeu, J.F., Costa, S.S., Bertola, D.R., Kim, C.A., Vianna-Morgante, A.M., Otto, P.A.

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Analysis of IL-1α, IL-1β, and IL-RA Polymorphisms in Dysthymia von Fertuzinhos, Sofia M. M., Oliveira, João R. M., Nishimura, Agnes L., Pontual, Deyse, Carvalho, Daniel R., Sougey, Everton B., Otto, Paulo A., Zatz, Mayana

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