检索结果 - Jacobs, Jennifer
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Method for appraising model validity of randomised controlled trials of homeopathic treatment: multi-rater concordance study 由 Mathie, Robert T, Roniger, Helmut, Van Wassenhoven, Michel, Frye, Joyce, Jacobs, Jennifer, Oberbaum, Menachem, Bordet, Marie-France, Nayak, Chaturbhuja, Chaufferin, Gilles, Ives, John A, Dantas, Flávio, Fisher, Peter
出版 2012Text -
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Real-World Performance of a Self-Operated Home Monitoring System for Early Detection of Neovascular Age-Related Macular Degeneration 由 Ho, Allen C., Heier, Jeffrey S., Holekamp, Nancy M., Garfinkel, Richard A., Ladd, Byron, Awh, Carl C., Singh, Rishi P., Sanborn, George E., Jacobs, Jennifer H., Elman, Michael J., Loewenstein, Anat, Eichenbaum, David A.
出版 2021Text -
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A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13 由 Leslie, Elizabeth J., Carlson, Jenna C., Shaffer, John R., Feingold, Eleanor, Wehby, George, Laurie, Cecelia A., Jain, Deepti, Laurie, Cathy C., Doheny, Kimberly F., McHenry, Toby, Resick, Judith, Sanchez, Carla, Jacobs, Jennifer, Emanuele, Beth, Vieira, Alexandre R., Neiswanger, Katherine, Lidral, Andrew C., Valencia-Ramirez, Luz Consuelo, Lopez-Palacio, Ana Maria, Valencia, Dora Rivera, Arcos-Burgos, Mauricio, Czeizel, Andrew E., Field, L. Leigh, Padilla, Carmencita D., Cutiongco-de la Paz, Eva Maria, C., Deleyiannis, Frederic, Christensen, Kaare, Munger, Ronald G., Lie, Rolv T., Wilcox, Allen, Romitti, Paul A., Castilla, Eduardo E., Mereb, Juan C., Poletta, Fernando A., Orioli, Iêda M., Carvalho, Flavia M., Hecht, Jacqueline T., Blanton, Susan H., Buxó, Carmen J., Butali, Azeez, Mossey, Peter A., Adeyemo, Wasiu L., James, Olutayo, Braimah, Ramat O., Aregbesola, Babatunde S., Eshete, Mekonen A., Abate, Fikre, Koruyucu, Mine, Seymen, Figen, Ma, Lian, de Salamanca, Javier Enríquez, Weinberg, Seth M., Moreno, Lina, Murray, Jeffrey C., Marazita, Mary L.
出版 2016Text -
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A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3 由 Leslie, Elizabeth J., Liu, Huan, Carlson, Jenna C., Shaffer, John R., Feingold, Eleanor, Wehby, George, Laurie, Cecelia A., Jain, Deepti, Laurie, Cathy C., Doheny, Kimberly F., McHenry, Toby, Resick, Judith, Sanchez, Carla, Jacobs, Jennifer, Emanuele, Beth, Vieira, Alexandre R., Neiswanger, Katherine, Standley, Jennifer, Czeizel, Andrew E., Deleyiannis, Frederic, Christensen, Kaare, Munger, Ronald G., Lie, Rolv T., Wilcox, Allen, Romitti, Paul A., Field, L. Leigh, Padilla, Carmencita D., Cutiongco-de la Paz, Eva Maria C., Lidral, Andrew C., Valencia-Ramirez, Luz Consuelo, Lopez-Palacio, Ana Maria, Valencia, Dora Rivera, Arcos-Burgos, Mauricio, Castilla, Eduardo E., Mereb, Juan C., Poletta, Fernando A., Orioli, Iêda M., Carvalho, Flavia M., Hecht, Jacqueline T., Blanton, Susan H., Buxó, Carmen J., Butali, Azeez, Mossey, Peter A., Adeyemo, Wasiu L., James, Olutayo, Braimah, Ramat O., Aregbesola, Babatunde S., Eshete, Mekonen A., Deribew, Milliard, Koruyucu, Mine, Seymen, Figen, Ma, Lian, de Salamanca, Javier Enríquez, Weinberg, Seth M., Moreno, Lina, Cornell, Robert A., Murray, Jeffrey C., Marazita, Mary L.
出版 2016Text