Resultats de la cerca - Levy, Brynn

Prenatal Diagnosis by Chromosomal Microarray Analysis per Levy, Brynn, Wapner, Ronald

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Noninvasive Prenatal Testing: The Future Is Now per Norwitz, Errol R, Levy, Brynn

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Trps1 and Its Target Gene Sox9 Regulate Epithelial Proliferation in the Developing Hair Follicle and Are Associated with Hypertrichosis per Fantauzzo, Katherine A., Kurban, Mazen, Levy, Brynn, Christiano, Angela M.

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Chromosomal Mosaicism: Origins and Clinical Implications in Preimplantation and Prenatal Diagnosis per Levy, Brynn, Hoffman, Eva, McCoy, Rajiv C., Grati, Francesca Romana

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SNP microarray-based 24 chromosome aneuploidy screening is significantly more consistent than FISH per Treff, Nathan R., Levy, Brynn, Su, Jing, Northrop, Lesley E., Tao, Xin, Scott, Richard T.

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3q27.1 microdeletion causes prenatal and postnatal growth restriction and neurodevelopmental abnormalities per Barua, Subit, Pereira, Elaine M., Jobanputra, Vaidehi, Anyane-Yeboa, Kwame, Levy, Brynn, Liao, Jun

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Glut1 Deficiency: Inheritance Pattern Determined by Haploinsufficiency per Rotstein, Michael, Engelstad, Kristin, Yang, Hong, Wang, Dong, Levy, Brynn, Chung, Wendy K., De Vivo, Darryl C.

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Incidental identification of balanced translocation carrier patients through comprehensive chromosome screening of IVF-derived blastocysts per Treff, Nathan R., Forman, Eric J., Katz-Jaffe, Mandy G., Schoolcraft, William B., Levy, Brynn, Scott, Richard T.

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Copy Number Variations on Chromosome 4q26–27 Are Associated with Cantu Syndrome per Kurban, Mazen, Kim, Chong Ae, Kiuru, Maija, Fantauzzo, Katherine, Cabral, Rita, Abbas, Ossama, Levy, Brynn, Christiano, Angela M.

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At the dawn of personalized reproductive medicine: opportunities and challenges with incorporating multigene panel testing into fertility care per Yurttas Beim, Piraye, Parfitt, David-Emlyn, Tan, Lei, Sugarman, Elaine A., Hu-Seliger, Tina, Clementi, Caterina, Levy, Brynn

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A rapid and simple bead-bashing-based method for genomic DNA extraction from mammalian tissue per Wei, Shan, Levy, Brynn, Hoffman, Nataly, Cujar, Claudia, Rodney-Sandy, Reunet, Wapner, Ronald, D'Alton, Mary, Williams, Zev

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Genome-wide analysis of abdominal and pleural malignant mesothelioma with DNA arrays reveals both common and distinct regions of copy number alteration per Borczuk, Alain C., Pei, Jianming, Taub, Robert N., Levy, Brynn, Nahum, Odelia, Chen, Jinli, Chen, Katherine, Testa, Joseph R.

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Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples per Ravi, Harini, McNeill, Gabriel, Goel, Shruti, Meltzer, Steven D., Hunkapiller, Nathan, Ryan, Allison, Levy, Brynn, Demko, Zachary P.

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Duplication of the ZIC2 gene is not associated with holoprosencephaly per Jobanputra, Vaidehi, Burke, Alanna, Kwame, Anyane-Yeboa, Shanmugham, Anita, Shirazi, Maryam, Brown, Stephen, Warburton, Peter E., Levy, Brynn, Warburton, Dorothy

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Prevalence and Physical Distribution of SRY in the gonads of a Woman with Turner Syndrome: Phenotypic Presentation, Tubal Formation, and Malignancy Risk per Baer, Tamar G., Freeman, Christopher E., Cujar, Claudia, Mansukhani, Mahesh, Singh, Bahadur, Chen, Xiaowei, Abellar, Rosanna, Oberfield, Sharon E, Levy, Brynn

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Case Report: Prenatal Identification of a De Novo Mosaic Neocentric Marker Resulting in 13q31.1→qter Tetrasomy in a Mildly Affected Girl per Dharmadhikari, Avinash V., Pereira, Elaine M., Andrews, Carli C ., Macera, Michael, Harkavy, Nina, Wapner, Ronald, Jobanputra, Vaidehi, Levy, Brynn, Ganapathi, Mythily, Liao, Jun

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Non-invasive prenatal aneuploidy testing at chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci per Zimmermann, Bernhard, Hill, Matthew, Gemelos, George, Demko, Zachary, Banjevic, Milena, Baner, Johan, Ryan, Allison, Sigurjonsson, Styrmir, Chopra, Nikhil, Dodd, Michael, Levy, Brynn, Rabinowitz, Matthew

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Genetic landscape of T- and NK-cell post-transplant lymphoproliferative disorders per Margolskee, Elizabeth, Jobanputra, Vaidehi, Jain, Preti, Chen, Jinli, Ganapathi, Karthik, Nahum, Odelia, Levy, Brynn, Morscio, Julie, Murty, Vundavalli, Tousseyn, Thomas, Alobeid, Bachir, Mansukhani, Mahesh, Bhagat, Govind

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Restoration of replication fork stability in BRCA1- and BRCA2-deficient cells by inactivation of SNF2-family fork remodelers per Taglialatela, Angelo, Alvarez, Silvia, Leuzzi, Giuseppe, Sannino, Vincenzo, Ranjha, Lepakshi, Huang, Jen-Wei, Madubata, Chioma, Anand, Roopesh, Levy, Brynn, Rabadan, Raul, Cejka, Petr, Costanzo, Vincenzo, Ciccia, Alberto

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Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions per Hensel, Charles, Vanzo, Rena, Martin, Megan, Dixon, Sean, Lambert, Christophe, Levy, Brynn, Nelson, Lesa, Peiffer, Andy, Ho, Karen S., Rushton, Patricia, Serrano, Moises, South, Sarah, Ward, Kenneth, Wassman, Edward

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