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

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Congenital extremity anomalies with a TBX5 pathogenic variant in consecutive IVF assisted pregnancies: a case report of Holt-Oram Syndrome by Sobh, Omar, O'Sullivan, Robert, Mahoney, Maurice J, Kleinman, Gary

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A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings by Chai, Hongyan, DiAdamo, Autumn, Grommisch, Brittany, Xu, Fang, Zhou, Qinghua, Wen, Jiadi, Mahoney, Maurice, Bale, Allen, McGrath, James, Spencer-Manzon, Michele, Li, Peining, Zhang, Hui

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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 by Rossi, Michael R., DiMaio, Miriam S., Xiang, Bixia, Lu, Kangmo, Kaymakcalan, Hande, Seashore, Margretta, Mahoney, Maurice J., Li, Peining

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Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization by 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 by 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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Hyperglycosylated Human Chorionic Gonadotropin (Invasive Trophoblast Antigen) Immunoassay: A New Basis for Gestational Down Syndrome Screening by 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 by 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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Antibiotic prophylaxis before amniocentesis by 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 by 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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The Mid-Trimester Genetic Sonogram by Bahado-Singh, Ray O., Oz, Utko A., Mendilcioglu, Inanc, Mahoney, Maurice J.

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

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Early genetic sonogram for down syndrome detection by Bahado-Singh, Ray O., Mendilcioglu, Inanc, Rowther, Minu, Choi, Sang-Joon, Oz, Utku, Yousefi, Nastaran Foyouzi, Mahoney, Maurice J.

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Association of extreme first-trimester free human chorionic gonadotropin-β, pregnancy-associated plasma protein A, and nuchal translucency with intrauterine growth restriction and... by Krantz, David, Goetzl, Laura, Simpson, Joe Leigh, Thom, Elizabeth, Zachary, Julia, Hallahan, Terrence W., Silver, Richard, Pergament, Eugene, Platt, Lawrence D., Filkins, Karen, Johnson, Anthony, Mahoney, Maurice, Hogge, W. Allen, Wilson, R. Douglas, Mohide, Patrick, Hershey, Douglas, Wapner, Ronald

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Combined serum and ultrasound screening for detection of fetal aneuploidy by Bahado-Singh, Ray, Cheng, Chih-Chien, Matta, Paul, Small, Maria, Mahoney, Maurice J.

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Comparison of urinary hyperglycosylated human chorionic gonadotropin concentration with the serum triple screen for Down syndrome detection in high-risk pregnancies by Bahado-Singh, Ray O., Oz, Utku, Shahabi, Shohreh, Mahoney, Maurice J., Baumgarten, Alexander, Cole, Laurence A.

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Ratio of nuchal thickness to humerus length for Down syndrome detection by Bahado-Singh, Ray O., Oz, Utku, Hsu, Char-Dong, Deren, Ozgur, Copel, Joshua A., Mahoney, Maurice J.

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First-trimester growth restriction and fetal aneuploidy: The effect of type of aneuploidy and gestational age by Bahado-Singh, Ray O., Lynch, Lauren, Deren, Ozgur, Morroti, Rafaella, Copel, Joshua A., Mahoney, Maurice J., Williams, John

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Cystic hygroma in the fetus and newborn by Gallagher, Patrick G., Mahoney, Maurice J., Gosche, John R.

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Genomic Characterization of Prenatal Detected Chromosomal Structural Abnormalities Using Oligonucleotide Array Comparative Genomic Hybridization by PEINING LI, POMIANOWSKI, Pawel, MAHONEY, Maurice J, DIMAIO, Miriam S, FLORIO, Joanne R, ROSSI, Michael R, BIXIA XIANG, FANG XU, HUI YANG, QIAN GENG, JIANSHENG XIE

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