Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Penelope A. Roberts"'
Publikováno v:
American Journal of Perinatology. 37:008-013
Objective To test the hypothesis that high fetal fraction (FF) on first trimester cell-free deoxyribonucleic acid (cfDNA) aneuploidy screening is associated with adverse perinatal outcomes. Study Design This is a single-institution retrospective coho
Autor:
Abigail Sassaman, Kathryn J. Gray, Lori Dobson, Michelle Pacione, Nancy J. Herrig, Lisa Dunn-Albanese, Sophie Adams, Samantha Gbur, Stephanie H. Guseh, Hayley Green, Chelsea Mandigo, Sarah B. Carroll, Kathleen Steinberg, Marie Discenza, Anjali J Kaimal, Judith Foster, Courtney Studwell, Marney Brillinger, Louise Wilkins-Haug, Penelope A. Roberts
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 23(7)
Copy-number variant (CNV) assessment is recommended for patients undergoing prenatal diagnostic testing. Noninvasive screening tests have not been extensively validated for CNV detection. The objective of this study was to compare the ability of geno
Autor:
Jennie P Mather, Penelope E Roberts, Zhuangyu Pan, Francine Chen, Jeffrey Hooley, Peter Young, Xiaolin Xu, Douglas H Smith, Ann Easton, Panjing Li, Ezio Bonvini, Scott Koenig, Paul A Moore
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e79456 (2013)
There is increasing evidence that many solid tumors are hierarchically organized with the bulk tumor cells having limited replication potential, but are sustained by a stem-like cell that perpetuates the tumor. These cancer stem cells have been hypot
Externí odkaz:
https://doaj.org/article/ecb298acd3e34a62b3cf7e4ba13bacf7
Autor:
Mark A. Clapp, Ilona T. Goldfarb, Lydia L. Shook, Sarah N. Bernstein, Margaret Berry, Penelope S. Roberts
Publikováno v:
American journal of perinatology. 37(1)
Objective To determine the association between low fetal fraction and birth weight among women with a negative cell-free DNA (cfDNA) result for common aneuploidies in the first trimester. Study Design This is a retrospective cohort of women who deliv
Autor:
Penelope A. Roberts
Publikováno v:
Patriarchy and Class ISBN: 9780429301155
Patriarchy and Class
Patriarchy and Class
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21c6c4f5df209c95e86d27714982ce68
https://doi.org/10.4324/9780429301155-5
https://doi.org/10.4324/9780429301155-5
Publikováno v:
American Journal of Obstetrics and Gynecology. 220:S163
Publikováno v:
American Journal of Obstetrics and Gynecology. 220:S583
Autor:
Rafaël Govaerts, Sven Buerki, Katherine Borland, Anne Tuomisto, Tony Hall, Maarten J. M. Christenhusz, Michael F. Fay, John David, Penelope S. Roberts, Mark W. Chase
Publikováno v:
Botanical Journal of the Linnean Society. 172:280-328
Tulipa (tulips; Liliaceae) is a genus of geophytes comprising c. 76 species, occurring from southwestern Europe and North Africa to Central Asia. The taxonomy and classification of the genus have been contentious in the past. We investigated the phyl
Autor:
Penelope S. Roberts, Małgorzata Tomyn-Drabik, Sergiusz Jóźwiak, Katarzyna Kotulska, Jolanta Kasprzyk-Obara, David J. Kwiatkowski, Dorota Domańska-Pakieła
Publikováno v:
Pediatrics. 118:e1146-e1151
OBJECTIVE. Tuberous sclerosis complex is an autosomal dominant disorder in which hamartomas occur in several organs. Cardiac rhabdomyomas, the most common heart tumors of childhood, are well known to be associated with tuberous sclerosis complex. Our
Autor:
Elizabeth A. Thiele, Penelope S. Roberts, S. Jozwiak, Joon Chung, David Neal Franz, David J. Kwiatkowski, Sandra L. Dabora
Publikováno v:
Human Genetics. 111:96-101
Inactivating mutations in the TSC2 gene, consisting of 41coding exons in 40 kb on 16p13, cause the hamartoma syndrome tuberous sclerosis. During TSC2 mutational analysis we identified ten SNPs that occur within or close to exon boundaries at minor al