نتائج البحث - Vengoechea, Jaime

De novo microduplication of the FMR1 gene in a patient with developmental delay, epilepsy and hyperactivity حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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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