Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Britton D. Rink"'
Autor:
Britton D. Rink
Publikováno v:
Prenatal Diagnosis. 43:489-495
Publikováno v:
Obstetrics & Gynecology. 140:121-131
Publikováno v:
Obstetrics and gynecology. 140(1)
Cell-free DNA is an advancing technology with increasing applications in screening, diagnosis, and treatment for several disease processes. The shared physiologic, genetic, and epigenetic characteristics of placental physiology and tumor development
Autor:
Joseph R. Biggio, Bryann Bromley, Lorraine Dugoff, P. Kaitlyn Edelson, Jessica L. Giordano, Anthony R. Gregg, Michael H. Guo, Stephanie Guseh, Susan Klugman, Jeffrey A. Kuller, Brynn Levy, Lauren Lichten, Tippi C. MacKenzie, Michael T. Mennuti, Quoc-Hung L. Nguyen, Mary E. Norton, Barbara M. O’Brien, Soha S. Patel, Malavika Prabhu, Sara Schonfeld Rabin-Havt, Aleksandar Rajkovic, Rebecca Reimers, Britton D. Rink, Melissa Stosic, Ignatia B. Van den Veyver, Ronald Wapner, Louise Wilkins-Haug, Russell G. Witt, Svetlana A. Yatsenko
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d32d45e4eacbce3b56e6992246b9ca68
https://doi.org/10.1016/b978-0-323-53094-1.01002-x
https://doi.org/10.1016/b978-0-323-53094-1.01002-x
Autor:
Britton D. Rink
Publikováno v:
Perinatal Genetics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5687d771395a3eb95f5bda31827e941
https://doi.org/10.1016/b978-0-323-53094-1.00003-5
https://doi.org/10.1016/b978-0-323-53094-1.00003-5
Autor:
Jeffrey A. Kuller, Britton D. Rink
Publikováno v:
Seminars in perinatology. 42(5)
Prenatal care providers are faced with a myriad of decisions about how to offer genetic screening and testing in ways that are appropriate to their patient population and their workflow. Among the critical issues brought to the forefront of rapidly a
Publikováno v:
Ibnosina Journal of Medicine and Biomedical Sciences. :27-30
Clinical ethical issues arise on a daily basis for medical clinicians. We report and discuss a case of an older minor. A 16-year old female, with a complicated clinical history following a heart transplant, developed irreversible complications from h
Autor:
Mary E. Norton, Britton D. Rink
Publikováno v:
Seminars in perinatology. 40(1)
Prenatal diagnostic testing is available for a growing number of disorders. The goal of prenatal diagnosis was initially focused on the identification of Down syndrome in women aged 35 years and older, but invasive prenatal genetic techniques can now
Autor:
Mary E. Norton, Britton D. Rink
Publikováno v:
Seminars in perinatology. 40(1)
Screening is currently recommended in pregnancy for a number of genetic disorders, chromosomal aneuploidy, and structural birth defects in the fetus regardless of maternal age or family history. There is an overwhelming array of sonographic and mater
Publikováno v:
Urology. 77:208-210
Beckwith-Wiedemann syndrome is a rare congenital overgrowth syndrome. It carries important connotations for the pediatric urologist because it is associated with an increased risk for developing certain embryonal tumors. Until recently, these patient