human sex ratio from conception to birth von Orzack, Steven Hecht, Stubblefield, J. William, Akmaev, Viatcheslav R., Colls, Pere, Munné, Santiago, Scholl, Thomas, Steinsaltz, David, Zuckerman, James E.

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Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens von Sugarman, Elaine A, Nagan, Narasimhan, Zhu, Hui, Akmaev, Viatcheslav R, Zhou, Zhaoqing, Rohlfs, Elizabeth M, Flynn, Kerry, Hendrickson, Brant C, Scholl, Thomas, Sirko-Osadsa, Deborah Alexa, Allitto, Bernice A

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Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis von Wapner, Ronald J, Martin, Christa Lese, Levy, Brynn, Ballif, Blake C, Eng, Christine M, Zachary, Julia M, Savage, Melissa, Platt, Lawrence D, Saltzman, Daniel, Grobman, William A, Klugman, Susan, Scholl, Thomas, Simpson, Joe Leigh, McCall, Kimberly, Aggarwal, Vimla S, Bunke, Brian, Nahum, Odelia, Patel, Ankita, Lamb, Allen N, Thom, Elizabeth A, Beaudet, Arthur L, Ledbetter, David H, Shaffer, Lisa G, Jackson, Laird

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BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast‐ovarian cancer von Hall, Michael J., Reid, Julia E., Burbidge, Lynn A., Pruss, Dmitry, Deffenbaugh, Amie M., Frye, Cynthia, Wenstrup, Richard J., Ward, Brian E., Scholl, Thomas A., Noll, Walter W.

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Amniotic fluid RNA gene expression profiling provides insights into the phenotype of Turner syndrome von Massingham, Lauren J., Johnson, Kirby L., Scholl, Thomas M., Slonim, Donna K., Wick, Heather C., Bianchi, Diana W.

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Clinical Characteristics of Individuals With Germline Mutations in BRCA1 and BRCA2: Analysis of 10,000 Individuals von Frank, T. S.

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Cystic Fibrosis Carrier Testing in an Ethnically Diverse US Population von ROHLFS, Elizabeth M, ZHAOQING ZHOU, SUGARMAN, Elaine A, HEIM, Ruth A, NAGAN, Narasimhan, ROSENBLUM, Lynne S, FLYNN, Kerry, SCHOLL, Thomas, AKMAEV, Viatcheslav R, SIRKO-OSADSA, D. Alexa, ALLITTO, Bernice A

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The visual analog scale allows effective measurement of preoperative Anxiety and detection of patients' anesthetic concerns von KINDLER, C. H, HARMS, C, AMSLER, F, IHDE-SCHOLL, T, SCHEIDEGGER, D

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Supplementary delta-rod configurations provide superior stiffness and reduced rod stress compared to traditional multiple-rod configurations after pedicle subtraction osteotomy: a... von Berjano, Pedro, Xu, Ming, Damilano, Marco, Scholl, Thomas, Lamartina, Claudio, Jekir, Michael, Galbusera, Fabio

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Specific Complex Formation between the Type II Bare Lymphocyte Syndrome-Associated Transactivators CIITA and RFX5 von Scholl, Thomas, Mahanta, Sanjeev K., Strominger, Jack L.

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Transactivation by CIITA, the Type II Bare Lymphocyte Syndrome-Associated Factor, Requires Participation of Multiple Regions of the TATA Box Binding Protein von Mahanta, Sanjeev K., Scholl, Thomas, Yang, Fu-Chia, Strominger, Jack L.

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Prediction of MLH1 and MSH2 Mutations in Lynch Syndrome von Balmaña, Judith, Stockwell, David H, Steyerberg, Ewout W, Stoffel, Elena M, Deffenbaugh, Amie M, Reid, Julia E, Ward, Brian, Scholl, Thomas, Hendrickson, Brant, Tazelaar, John, Burbidge, Lynn Anne, Syngal, Sapna

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Genetic heterozygosity and pseudodeficiency in the Pompe disease newborn screening pilot program von Labrousse, Paul, Chien, Yin-Hsiu, Pomponio, Robert J., Keutzer, Joan, Lee, Ni-Chung, Akmaev, Viatcheslav R., Scholl, Thomas, Hwu, Wuh-Liang

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Shared Genetic Susceptibility to Breast Cancer, Brain Tumors, and Fanconi Anemia von Offit, Kenneth, Levran, Orna, Mullaney, Brian, Mah, Katherine, Nafa, Khedoudja, Batish, Sat Dev, Diotti, Raffaella, Schneider, Hildegard, Deffenbaugh, Amie, Scholl, Thomas, Proud, Virginia K., Robson, Mark, Norton, Larry, Ellis, Nathan, Hanenberg, Helmut, Auerbach, Arleen D.

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Multiple Rare Nonsynonymous Variants in the Adenomatous Polyposis Coli Gene Predispose to Colorectal Adenomas von AZZOPARDI, Duncan, DALLOSSO, Anthony R, WENSTRUP, Richard, SCHOLL, Thomas, CHEADLE, Jeremy P, ELIASON, Kristilyn, HENDRICKSON, Brant C, JONES, Natalie, RAWSTORNE, Edward, COLLEY, James, MOSKVINA, Valentina, FRYE, Cynthia, SAMPSON, Julian R

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Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa von Sangaré, Modibo, Hendrickson, Brant, Sango, Hammadoun Ali, Chen, Kelian, Nofziger, Jonathan, Amara, Abdelbasset, Dutra, Amalia, Schindler, Alice B., Guindo, Aldiouma, Traoré, Mahamadou, Harmison, George, Pak, Evgenia, Yaro, Fatoumata N'Go, Bricceno, Katherine, Grunseich, Christopher, Chen, Guibin, Boehm, Manfred, Zukosky, Kristen, Bocoum, Nouhoum, Meilleur, Katherine G., Daou, Fatoumata, Bagayogo, Koumba, Coulibaly, Yaya Ibrahim, Diakité, Mahamadou, Fay, Michael P., Lee, Hee-Suk, Saad, Ali, Gribaa, Moez, Singleton, Andrew B., Maiga, Youssoufa, Auh, Sungyoung, Landouré, Guida, Fairhurst, Rick M., Burnett, Barrington G., Scholl, Thomas, Fischbeck, Kenneth H.

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Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia von Wagner, John E., Tolar, Jakub, Levran, Orna, Scholl, Thomas, Deffenbaugh, Amie, Satagopan, Jaya, Ben-Porat, Leah, Mah, Katherine, Batish, Sat Dev, Kutler, David I., MacMillan, Margaret L., Hanenberg, Helmut, Auerbach, Arleen D.

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SYSTEMS AND METHODS FOR PLANNING, PERFORMING, AND ASSESSING SPINAL CORRECTION DURING SURGERY von Scholl, Thomas

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Systems and methods for planning, performing, and assessing spinal correction during surgery von Scholl, Thomas

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Development of a Pompe disease CRIM assay for blood samples von Keutzer, Joan, Wang, Zhaohui, Okamoto, Patricia, Scholl, Thomas

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