Noninvasive Prenatal Testing and Detection of Maternal Cancer von Romero, Roberto, Mahoney, Maurice J

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Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: Study of two cases and review of the literature von Rossi, Michael R., DiMaio, Miriam S., Xiang, Bixia, Lu, Kangmo, Kaymakcalan, Hande, Seashore, Margretta, Mahoney, Maurice J., Li, Peining

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Sequential pathways of testing after first-trimester screening for trisomy 21 von PLATT, Lawrence D, GREENE, Naomi, PERGAMENT, Eugene, FILKINS, Karen, MAHONEY, Maurice J, HOGGE, W. Allen, WILSON, R. Douglas, MOHIDE, Patrick, HERSHEY, Douglas, MACGREGOR, Scott, BAHADO-SINGH, Ray, JACKSON, Laird G, JOHNSON, Anthony, WAPNER, Ronald, ZACHARY, Julia, THOM, Elizabeth, KRANTZ, David, SIMPSON, Joe Leigh, SILVER, Richard K, SNIJDERS, Rosalinde J. M, GOETZL, Laura

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Maternal plasma DNA testing for aneuploidy in pregnancies achieved by assisted reproductive technologies von Lambert-Messerlian, Geralyn, Kloza, Edward M., Williams, John, Loucky, Jaroslav, O’Brien, Barbara, Wilkins-Haug, Louise, Mahoney, Maurice J., De Biasio, Pierangela, Borrell, Antoni, Ehrich, Mathias, van den Boom, Dirk, Bombard, Allan T., Deciu, Cosmin, Palomaki, Glenn E.

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Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization von Li, Peining, Pomianowski, Pawel, DiMaio, Miriam S., Florio, Joanne R., Rossi, Michael R., Xiang, Bixia, Xu, Fang, Yang, Hui, Geng, Qian, Xie, Jiansheng, Mahoney, Maurice J.

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Elevated first-trimester nuchal translucency increases the risk of congenital heart defects von Bahado-Singh, Ray O., Wapner, Ronald, Thom, Elizabeth, Zachary, Julia, Platt, Lawrence, Mahoney, Maurice J., Johnson, Anthony, Silver, Richard K., Pergament, Eugene, Filkins, Karen, Hogge, W. Allen, Wilson, R. Douglas, Jackson, Laird G.

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Pregnancy-associated plasma protein A, free β-hCG, nuchal translucency, and risk of pregnancy loss von GOETZL, Laura, KRANTZ, David, SIMPSON, Joe Leigh, SILVER, Richard K, ZACHARY, Julia M, PERGAMENT, Eugene, PLATT, Lawrence D, MAHONEY, Maurice J, WAPNER, Ronald J

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Fragile X syndrome carrier screening in the prenatal genetic counseling setting von Cronister, Amy, DiMaio, Miriam, Mahoney, Maurice J., Donnenfeld, Alan E., Hallam, Stephanie

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Hyperglycosylated Human Chorionic Gonadotropin (Invasive Trophoblast Antigen) Immunoassay: A New Basis for Gestational Down Syndrome Screening von Cole, Laurence A, Shahabi, Shohreh, Oz, Utku A, Bahado-Singh, Ray O, Mahoney, Maurice J

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Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848 von Koczkowska, Magdalena, Chen, Yunjia, Callens, Tom, Gomes, Alicia, Sharp, Angela, Johnson, Sherrell, Hsiao, Meng-Chang, Chen, Zhenbin, Balasubramanian, Meena, Barnett, Christopher P., Becker, Troy A., Ben-Shachar, Shay, Bertola, Debora R., Blakeley, Jaishri O., Burkitt-Wright, Emma M.M., Callaway, Alison, Crenshaw, Melissa, Cunha, Karin S., Cunningham, Mitch, D’Agostino, Maria D., Dahan, Karin, De Luca, Alessandro, Destrée, Anne, Dhamija, Radhika, Eoli, Marica, Evans, D. Gareth R., Galvin-Parton, Patricia, George-Abraham, Jaya K., Gripp, Karen W., Guevara-Campos, Jose, Hanchard, Neil A., Hernández-Chico, Concepcion, Immken, LaDonna, Janssens, Sandra, Jones, Kristi J., Keena, Beth A., Kochhar, Aaina, Liebelt, Jan, Martir-Negron, Arelis, Mahoney, Maurice J., Maystadt, Isabelle, McDougall, Carey, McEntagart, Meriel, Mendelsohn, Nancy, Miller, David T., Mortier, Geert, Morton, Jenny, Pappas, John, Plotkin, Scott R., Pond, Dinel, Rosenbaum, Kenneth, Rubin, Karol, Russell, Laura, Rutledge, Lane S., Saletti, Veronica, Schonberg, Rhonda, Schreiber, Allison, Seidel, Meredith, Siqveland, Elizabeth, Stockton, David W., Trevisson, Eva, Ullrich, Nicole J., Upadhyaya, Meena, van Minkelen, Rick, Verhelst, Helene, Wallace, Margaret R., Yap, Yoon-Sim, Zackai, Elaine, Zonana, Jonathan, Zurcher, Vickie, Claes, Kathleen, Martin, Yolanda, Korf, Bruce R., Legius, Eric, Messiaen, Ludwine M.

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LabCorp v. Metabolite Laboratories: The Supreme Court Listens, but Declines to Speak von Klein, Roger D., Mahoney, Maurice J.

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Late First-Trimester Placental Disruption and Subsequent Gestational Hypertension/Preeclampsia von Silver, Richard K, Wilson, R Douglas, Philip, John, Thom, Elizabeth A, Zachary, Julia M, Mohide, Patrick, Mahoney, Maurice J, Simpson, Joe L, Platt, Larry D, Pergament, Eugene, Hershey, Douglas, Filkins, Karen, Johnson, Anthony, Wapner, Ronald J, Jackson, Laird G

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Antibiotic prophylaxis before amniocentesis von Hobbins, John C., Pilu, Gianluigi, Abuhumad, Alfred, Alfirevic, Zarko, Bahado-Singh, Ray O., Benacerraf, Beryl R., Berkowitz7, Richard L., Cetin, Irene, Copel, Joshua A., Eik-Nes, Sturla, Frusca, Tiziana, Galan, Henry L., Guaschino, Secondo, Mahoney, Maurice J., Marsal, Karel, Malinger, Gustavo, Marconi, Anna Maria, Martinelli, Pasquale, Moore, Thomas R., Papageorghiou, Aris T., Platt, Lawrence D., Rizzo, Nicola, Tabor, Ann, Thilaganathan, Baskaran, Timor-Tritsch, Ilan E., Todros, Tullia, Yagel, Simcha

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Variable Expression of a Novel PLP1 Mutation in Members of a Family With Pelizaeus-Merzbacher Disease von Fattal-Valevski, Aviva, DiMaio, Miriam S., Hisama, Fuki M., Hobson, Grace M., Davis-Williams, Angelique, Garbern, James Y., Mahoney, Maurice J., Kolodny, Edwin H., Pastores, Gregory M.

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Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation von Koczkowska, Magdalena, Callens, Tom, Gomes, Alicia, Sharp, Angela, Chen, Yunjia, Hicks, Alesha D., Aylsworth, Arthur S., Azizi, Amedeo A., Basel, Donald G., Bellus, Gary, Bird, Lynne M., Blazo, Maria A., Burke, Leah W., Cannon, Ashley, Collins, Felicity, DeFilippo, Colette, Denayer, Ellen, Digilio, Maria C., Dills, Shelley K., Dosa, Laura, Greenwood, Robert S., Griffis, Cristin, Gupta, Punita, Hachen, Rachel K., Hernández-Chico, Concepción, Janssens, Sandra, Jones, Kristi J., Jordan, Justin T., Kannu, Peter, Korf, Bruce R., Lewis, Andrea M., Listernick, Robert H., Lonardo, Fortunato, Mahoney, Maurice J., Ojeda, Mayra Martinez, McDonald, Marie T., McDougall, Carey, Mendelsohn, Nancy, Miller, David T., Mori, Mari, Oostenbrink, Rianne, Perreault, Sebastién, Pierpont, Mary Ella, Piscopo, Carmelo, Pond, Dinel A., Randolph, Linda M., Rauen, Katherine A., Rednam, Surya, Rutledge, S. Lane, Saletti, Veronica, Schaefer, G. Bradley, Schorry, Elizabeth K., Scott, Daryl A., Shugar, Andrea, Siqveland, Elizabeth, Starr, Lois J., Syed, Ashraf, Trapane, Pamela L., Ullrich, Nicole J., Wakefield, Emily G., Walsh, Laurence E., Wangler, Michael F., Zackai, Elaine, Claes, Kathleen B. M., Wimmer, Katharina, van Minkelen, Rick, De Luca, Alessandro, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine M.

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Proteomics: A Novel Methodology to Complement Prenatal Diagnosis of Chromosomal Abnormalities and Inherited Human Diseases von Bahtiyar, Mert Ozan, Copel, Joshua A, Mahoney, Maurice J, Buhimschi, Irina A, Buhimschi, Catalin S

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The Mid-Trimester Genetic Sonogram von Bahado-Singh, Ray O., Oz, Utko A., Mendilcioglu, Inanc, Mahoney, Maurice J.

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The Natural History of the Inherited Methylmalonic Acidemias von Matsui, Suzanne M, Mahoney, Maurice J, Rosenberg, Leon E

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The comprehensive midtrimester test: High-sensitivity down syndrome test von Bahado-Singh, Ray, Shahabi, Shohreh, Karaca, Mehmet, Mahoney, Maurice J., Cole, Laurence, Oz, Utku A.

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The Safety and Efficacy of Chorionic Villus Sampling for Early Prenatal Diagnosis of Cytogenetic Abnormalities von Rhoads, George G, Jackson, Laird G, Schlesselman, Sarah E, de la Cruz, Felix F, Desnick, Robert J, Golbus, Mitchell S, Ledbetter, David H, Lubs, Herbert A, Mahoney, Maurice J, Pergament, Eugene, Simpson, Joe Leigh, Carpenter, Robert J, Elias, Sherman, Ginsberg, Norman A, Goldberg, James D, Hobbins, John C, Lynch, Lauren, Shiono, Patricia H, Wapner, Ronald J, Zachary, Julia M

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