Genetic testing by cancer site: ovary von Weissman, Scott M, Weiss, Shelly M, Newlin, Anna C

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Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice von Selkirk, Christina G., Vogel, Kristen J., Newlin, Anna C., Weissman, Scott M., Weiss, Shelly M., Wang, Chi-Hsiung, Hulick, Peter J.

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10 rare tumors that warrant a genetics referral von Banks, Kimberly C., Moline, Jessica J., Marvin, Monica L., Newlin, Anna C., Vogel, Kristen J.

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Psychological impact of recall in high-risk breast MRI screening von O'Neill, Suzanne M, Rubinstein, Wendy S, Sener, Stephen F, Weissman, Scott M, Newlin, Anna C, West, Daniel K, Ecanow, David B, Rademaker, Alfred W, Edelman, Robert R

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Handbook of Pediatric Eye and Systemic Disease von Wright, Kenneth W, Spiegel, Peter H, Thompson, Lisa S

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Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance von Tischfield, Max A., Baris, Hagit N., Wu, Chen, Rudolph, Guenther, Van Maldergem, Lionel, He, Wei, Chan, Wai-Man, Andrews, Caroline, Demer, Joseph L., Robertson, Richard L., Mackey, David A., Ruddle, Jonathan B., Bird, Thomas D., Gottlob, Irene, Pieh, Christina, Traboulsi, Elias I., Pomeroy, Scott L., Hunter, David G., Soul, Janet S., Newlin, Anna, Sabol, Louise J., Doherty, Edward J., de Uzcátegui, Clara E., de Uzcátegui, Nicolas, Collins, Mary Louise Z., Sener, Emin C., Wabbels, Bettina, Hellebrand, Heide, Meitinger, Thomas, de Berardinis, Teresa, Magli, Adriano, Schiavi, Costantino, Pastore-Trossello, Marco, Koc, Feray, Wong, Agnes M., Levin, Alex V., Geraghty, Michael T., Descartes, Maria, Flaherty, Maree, Jamieson, Robyn V., Møller, H.U., Meuthen, Ingo, Callen, David F., Kerwin, Janet, Lindsay, Susan, Meindl, Alfons, Gupta, Mohan L., Pellman, David, Engle, Elizabeth C.

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Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant von Li, Jun, Woods, Susan L., Healey, Sue, Beesley, Jonathan, Chen, Xiaoqing, Lee, Jason S., Sivakumaran, Haran, Wayte, Nicci, Nones, Katia, Waterfall, Joshua J., Pearson, John, Patch, Anne-Marie, Senz, Janine, Ferreira, Manuel A., Kaurah, Pardeep, Mackenzie, Robertson, Heravi-Moussavi, Alireza, Hansford, Samantha, Lannagan, Tamsin R.M., Spurdle, Amanda B., Simpson, Peter T., da Silva, Leonard, Lakhani, Sunil R., Clouston, Andrew D., Bettington, Mark, Grimpen, Florian, Busuttil, Rita A., Di Costanzo, Natasha, Boussioutas, Alex, Jeanjean, Marie, Chong, George, Fabre, Aurélie, Olschwang, Sylviane, Faulkner, Geoffrey J., Bellos, Evangelos, Coin, Lachlan, Rioux, Kevin, Bathe, Oliver F., Wen, Xiaogang, Martin, Hilary C., Neklason, Deborah W., Davis, Sean R., Walker, Robert L., Calzone, Kathleen A., Avital, Itzhak, Heller, Theo, Koh, Christopher, Pineda, Marbin, Rudloff, Udo, Quezado, Martha, Pichurin, Pavel N., Hulick, Peter J., Weissman, Scott M., Newlin, Anna, Rubinstein, Wendy S., Sampson, Jone E., Hamman, Kelly, Goldgar, David, Poplawski, Nicola, Phillips, Kerry, Schofield, Lyn, Armstrong, Jacqueline, Kiraly-Borri, Cathy, Suthers, Graeme K., Huntsman, David G., Foulkes, William D., Carneiro, Fatima, Lindor, Noralane M., Edwards, Stacey L., French, Juliet D., Waddell, Nicola, Meltzer, Paul S., Worthley, Daniel L., Schrader, Kasmintan A., Chenevix-Trench, Georgia

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Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1) von Engle, Elizabeth C, Yamada, Koki, Andrews, Caroline, Chan, Wai-Man, McKeown, Craig A, Magli, Adriano, de Berardinis, Teresa, Loewenstein, Anat, Lazar, Moshe, O'Keefe, Michael, Letson, Robert, London, Arnold, Ruttum, Mark, Matsumoto, Naomichi, Saito, Nakamichi, Morris, Lisa, Monte, Monte Del, Johnson, Roger H, Uyama, Eiichiro, Houtman, Willem A, de Vries, Berendina, Carlow, Thomas J, Hart, Blaine L, Krawiecki, Nicolas, Shoffner, John, Vogel, Marlene C, Katowitz, James, Goldstein, Scott M, Levin, Alex V, Sener, Emin C, Ozturk, Banu T, Akarsu, A Nurten, Brodsky, Michael C, Hanisch, Frank, Cruse, Robert P, Zubcov, Alina A, Robb, Richard M, Roggenkäemper, Peter, Gottlob, Irene, Kowal, Lionel, Battu, Ravi, Traboulsi, Elias I, Franceschini, Piergiorgio, Newlin, Anna, Demer, Joseph L

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Advances in counselling and surveillance of patients at risk for pancreatic cancer von Brand, Randall E, Lerch, Markus M, Rubinstein, Wendy S, Neoptolemos, John P, Whitcomb, David C, Hruban, Ralph H, Brentnall, Teresa A, Lynch, Henry T, Canto, Marcia I

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Characterization and Prevalence of PITX2 Microdeletions and Mutations in Axenfeld-Rieger Malformations von Lines, Matthew A, Kozlowski, Kathy, Kulak, Stephen C, Allingham, R. Rand, Heon, Elise, Ritch, Robert, Levin, Alex V, Shields, M. Bruce, Damji, Karim F, Newlin, Anna, Walter, Michael A

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