Pseudoautosomal abnormalities in terminal AZFb+c deletions are associated with isochromosomes Yp and may lead to abnormal growth and neuropsychiatric function von Castro, A., Rodríguez, F., Flórez, M., López, P., Curotto, B., Martínez, D., Maturana, A., Lardone, M.C., Palma, C., Mericq, V., Ebensperger, M., Cassorla, F.

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FXTAS in an unmethylated mosaic male with fragile X syndrome from Chile von Santa María, L., Pugin, A., Alliende, M.A., Aliaga, S., Curotto, B., Aravena, T., Tang, H.-T., Mendoza-Morales, G., Hagerman, R., Tassone, F.

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Clinical, molecular, and pharmacological aspects of FMR1-related disorders von Pugin, A., Faundes, V., Santa María, L., Curotto, B., Aliaga, S., Salas, I., Soto, P., Bravo, P., Peña, M.I., Alliende, M.A.

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Aspectos clínicos, moleculares y farmacológicos en los trastornos asociados a gen 1 del retraso mental del X frágil von Pugin, A, Faundes, V, Santa María, L, Curotto, B, Aliaga, S, Salas, I, Soto, P, Bravo, P, Peña, M.I, Alliende, M.A

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CARACTERIZACIÓN MOLECULAR DE CARIOTIPO DESBALANCEADO 45,X,add(13)(p10) DE HOMBRE CON AZOOSPERMIA von Pena, A, Curotto, B, Morales, P, Quiroga, A, Faúndes, V

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Clinical and Cytogenetical diagnosis in the Fragil X Syndrome von Cortés, F, Curotto, B, Rios, L, Barrios, A, Alliende, M A

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Barber-Say syndrome: further delineation of the clinical spectrum von Cortés, Fanny M., Troncoso, Ledia A., Alliende, Angélica R., Curotto, Bianca L.

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Cytogenetic and molecular profile of genetic diseases in Puerto Montt main hospital von Alliende, M Angélica, Curotto, Bianca, Guerra, Patricio, Santa María, Lorena, Hermosilla, Reinería, Orphanópoulos, Doris, Villanueva, Jorge, Wettig, Elizabeth, Barraza, Ximena

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Genetic screening to determine an etiologic diagnosis in children with mental retardation von Alliende, M Angélica, Cámpora, Laura, Curotto, Bianca, Toro, Jessica, Valiente, Alf, Castillo, Marcela, Cortés, Fanny, Trigo, César, Alvarado, Cecilia, Silva, Manuel, Caru, Margarita

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Clinical, genetic and molecular features in 45 patients with Prader-Willi syndrome von Cortés M, Fanny, Alliende R, M Angélica, Barrios R, Andrés, Curotto L, Bianca, Santa María V, Lorena, Barraza O, Ximena, Troncoso A, Ledia, Mellado S, Cecilia, Pardo V, Rosa

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Molecular diagnosis of Prader-Willi and Angelman syndromes: methylation, cytogenetics and FISH analysis von Santa María, L, Curotto, B, Cortés, F, Rojas, C, Alliende, M A

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Direct molecular analysis of FMR-1 gene mutation in patients with fragile Xq syndrome and their families von Alliende, M A, Urzúa, B, Valiente, A, Cortés, F, Curotto, B, Rojas, C

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Prader-Willi syndrome due to 15q11-q13 deletion in a girl with an inherited (13;14) Robertsonian translocation von Alliende, Angélica, Curotto, Bianca, Maria, Lorena Santa, Cortés, Fanny, Aracena, Mariana

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Cytogenetic findings in patients with Down's syndrome von Cortés, F, Alliende, M, Curotto, B

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Neuropilin 1 is expressed on thymus-derived natural regulatory T cells, but not mucosa-generated induced Foxp3+ T reg cells von Weiss, Jonathan M, Bilate, Angelina M, Gobert, Michael, Ding, Yi, Curotto de Lafaille, Maria A, Parkhurst, Christopher N, Xiong, Huizhong, Dolpady, Jayashree, Frey, Alan B, Ruocco, Maria Grazia, Yang, Yi, Floess, Stefan, Huehn, Jochen, Oh, Soyoung, Li, Ming O, Niec, Rachel E, Rudensky, Alexander Y, Dustin, Michael L, Littman, Dan R, Lafaille, Juan J

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Clinical and immunochemical profiles of food challenge proven or anaphylactic shrimp allergy in tropical Singapore von Thalayasingam, M., Gerez, I. F. A., Yap, G. C., Llanora, G. V., Chia, I. P., Chua, L., Lee, C. J. A. O., Ta, L. D. H., Cheng, Y. K., Thong, B. Y. H., Tang, C. Y., Van Bever, H. P. S., Shek, L. P., Curotto de Lafaille, M. A., Lee, B. W.

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The differential diagnosis of syndromes of bone marrow hypoplasia associated with malformation of the extremities von Curotto, B, Alliende, M A, Lacassie, Y

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Diesel Exhaust Particle-Exposed Human Bronchial Epithelial Cells Induce Dendritic Cell Maturation von Bleck, Bertram, Tse, Doris B, Jaspers, Ilona, Curotto de Lafaille, Maria A, Reibman, Joan

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Diesel Exhaust Particle-Exposed Human Bronchial Epithelial Cells Induce Dendritic Cell Maturation and Polarization via Thymic Stromal Lymphopoietin von Bleck, Bertram, Tse, Doris B., Curotto de Lafaille, Maria A., Zhang, Feijie, Reibman, Joan

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Expression profiles of regulatory and helper T-cell-associated genes in nasal polyposis von Li, C. W., Zhang, K. K., Li, T. Y., Lin, Z. B., Li, Y. Y., Curotto de Lafaille, M. A., Shi, L., Wang, D. Y.

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