检索结果 - Vengoechea, Jaime

De novo microduplication of the FMR1 gene in a patient with developmental delay, epilepsy and hyperactivity 由 Vengoechea, Jaime, Parikh, Aditi S, Zhang, Shulin, Tassone, Flora

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Duplication of the ALDH1A2 gene in association with pentalogy of Cantrell: a case report 由 Steiner, Matthew B, Vengoechea, Jaime, Collins, Ronnie Thomas

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A rare mutation in hypophosphatasia: a case report of adult form and review of the literature 由 Galeano-Valle, Francisco, Vengoechea, Jaime, Galindo, Rodolfo J.

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Description of the First Case of Adenomyomatosis of the Gallbladder in an Infant 由 Zarate, Yuri A., Bosanko, Katherine A., Jarasvaraparn, Chaowapong, Vengoechea, Jaime, McDonough, Elizabeth M.

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Association of metabolic syndrome with glioblastoma: a retrospective cohort study and review 由 Rogers, Lisa R, Ostrom, Quinn T, Schroer, Julia, Vengoechea, Jaime, Li, Li, Gerson, Stanton, Nock, Charles J, Machtay, Mitchell, Selman, Warren, Lo, Simon, Sloan, Andrew E, Barnholtz-Sloan, Jill S

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A nomogram for individualized estimation of survival among patients with brain metastasis 由 Barnholtz-Sloan, Jill S., Yu, Changhong, Sloan, Andrew E., Vengoechea, Jaime, Wang, Meihua, Dignam, James J., Vogelbaum, Michael A., Sperduto, Paul W., Mehta, Minesh P., Machtay, Mitchell, Kattan, Michael W.

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Clinical Report: Germline Mosaicism in Cornelia de Lange Syndrome 由 Slavin, Thomas P., Lazebnik, Noam, Clark, Dinah M., Vengoechea, Jaime, Cohen, Leslie, Kaur, Maninder, Konczal, Laura, Crowe, Carol A., Corteville, Jane E., Nowaczyk, Malgorzata J., Byrne, Janice L., Jackson, Laird G., Krantz, Ian D.

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Variation In Age At Cancer Diagnosis In Familial Versus Non-Familial Barrett’s Esophagus 由 Chak, Amitabh, Chen, Yanwen, Vengoechea, Jaime, Canto, Marcia I., Elston, Robert, Falk, Gary W., Grady, William M., Guda, Kishore, Kinnard, Margaret, Markowitz, Sanford, Mittal, Sumeet, Prasad, Ganapathy, Shaheen, Nicholas, Willis, Joseph E., Barnholtz-Sloan, Jill

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Molecular Subtypes of Glioblastoma Are Relevant to Lower Grade Glioma 由 Guan, Xiaowei, Vengoechea, Jaime, Zheng, Siyuan, Sloan, Andrew E., Chen, Yanwen, Brat, Daniel J., O’Neill, Brian Patrick, de Groot, John, Yust-Katz, Shlomit, Yung, Wai-Kwan Alfred, Cohen, Mark L., Aldape, Kenneth D., Rosenfeld, Steven, Verhaak, Roeland G. W., Barnholtz-Sloan, Jill S.

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A variable age of onset segregation model for linkage analysis, with correction for ascertainment, applied to glioma 由 Sun, Xiangqing, Vengoechea, Jaime, Elston, Robert, Chen, Yanwen, Amos, Christopher I., Armstrong, Georgina, Bernstein, Jonine L, Claus, Elizabeth, Davis, Faith, Houlston, Richard S, Il'yasova, Dora, Jenkins, Robert B, Johansen, Christoffer, Lai, Rose, Lau, Ching C, Liu, Yanhong, McCarthy, Bridget J, Olson, Sara H, Sadetzki, Siegal, Schildkraut, Joellen, Shete, Sanjay, Yu, Robert, Vick, Nicholas A, Merrell, Ryan, Wrensch, Margaret, Yang, Ping, Melin, Beatrice, Bondy, Melissa L., Barnholtz-Sloan, Jill S.

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Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency 由 Saettini, Francesco, Poli, Cecilia, Vengoechea, Jaime, Bonanomi, Sonia, Orellana, Julio C., Fazio, Grazia, Rodriguez, Fred H., Noguera, Loreani P., Booth, Claire, Jarur-Chamy, Valentina, Shams, Marissa, Iascone, Maria, Vukic, Maja, Gasperini, Serena, Quadri, Manuel, Barroeta Seijas, Amairelys, Rivers, Elizabeth, Mauri, Mario, Badolato, Raffaele, Cazzaniga, Gianni, Bugarin, Cristina, Gaipa, Giuseppe, Kroes, Wilma G. M., Moratto, Daniele, van Oostaijen-ten Dam, Monique M., Baas, Frank, van der Maarel, Silvère, Piazza, Rocco, Coban-Akdemir, Zeynep H., Lupski, James R., Yuan, Bo, Chinn, Ivan K., Daxinger, Lucia, Biondi, Andrea

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