Search Results - Levy, Brynn

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

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Noninvasive Prenatal Testing: The Future Is Now by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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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