Mosaic trisomy 16 ascertained through amniocentesis: Evaluation of 11 new cases by Hsu, Wei-Tong, Shchepin, Dmitriy A., Mao, Rong, Berry-Kravis, Elizabeth, Garber, Ann P., Fischel-Ghodsian, Nathan, Falk, Rena E., Carlson, Dru E., Roeder, Elizabeth R., Leeth, Elizabeth A., Hajianpour, M.J., Wang, Jin-Chen C., Rosenblum-Vos, Lynne S., Bhatt, Sucheta D., Karson, Evelyn M., Hux, Charles H., Trunca, Carolyn, Bialer, Martin G., Linn, Sandra K., Schreck, Rhona R.

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Performance of a Paired-End Sequencing-Based Noninvasive Prenatal Screening Test in the Detection of Genome-Wide Fetal Chromosomal Anomalies by Pertile, Mark D, Flowers, Nicola, Vavrek, Darcy, Andrews, Daniel, Kalista, Tasha, Craig, Andrew, Deciu, Cosmin, Duenwald, Sven, Meier, Kristen, Bhatt, Sucheta

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Evaluation of an automated process for disclosure of negative noninvasive prenatal test results by Kalejta, Cassidi D., Higgins, Sonja, Kershberg, Hilary, Greenberg, Jeff, Alvarado, Monica, Cooke, Kerry, Bhatt, Sucheta, Bulpitt, Denise, Armour, Jamie, Bejjani, Bassem, Ryan, Shawnia, Elms, Amanda

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Vaccine storage practices in pediatric offices by Bishai, D M, Bhatt, S, Miller, L T, Hayden, G F

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Deletions of 20p12 in Alagille syndrome: Frequency and molecular characterization by Krantz, Ian D., Rand, Elizabeth B., Genin, Anna, Hunt, Piper, Jones, Marilyn, Louis, Anthonise A., Graham Jr, John M., Bhatt, Sucheta, Piccoli, David A., Spinner, Nancy B.

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