Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Buller-Burckle A"'
Autor:
Rebecca Nakles-Taylor, Elinette Albino, David Tsao, Rebecca Chen, Camille Nery, Izabela Karbassi, Arlene Buller-Burckle
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100434- (2023)
Externí odkaz:
https://doaj.org/article/420939d1afec45208a02f325576ac86a
Autor:
Nakles-Taylor, Rebecca, Albino, Elinette, Tsao, David, Chen, Rebecca, Nery, Camille, Karbassi, Izabela, Buller-Burckle, Arlene
Publikováno v:
In Genetics in Medicine Open 2023 1(1) Supplement
Autor:
Kalman, Lisa V., Tarleton, Jack C., Percy, Alan K., Aradhya, Swaroop, Bale, Sherri, Barker, Shannon D., Bayrak-Toydemir, Pinar, Bridges, Christina, Buller-Burckle, Arlene M., Das, Soma, Iyer, Ramaswamy K., Vo, Timothy D., Zvereff, Val V., Toji, Lorraine H.
Publikováno v:
In The Journal of Molecular Diagnostics March 2014 16(2):273-279
Autor:
Hantash, Feras M. *, Goos, Dana G., Tsao, David, Quan, Franklin, Buller-Burckle, Arlene, Peng, Mei, Jarvis, Michael, Sun, Weimin, Strom, Charles M.
Publikováno v:
In Genetics in Medicine March 2010 12(3):162-173
Autor:
Weimin Sun, Renius Owen, Sun Hee Rosenthal, Arlene Buller-Burckle, Quoclinh Nguyen, Ke Zhang, James Li, David Wolfson, Elaine Hiller, Anna Gerasimova, Christopher Elzinga, Linda Cheng, Andrew Grupe, Alla Smolgovsky, Rebecca Chen, Joseph J. Catanese, Carolyn Castonguay, Yan Liu, Camille R. Nery, Felicitas Lacbawan
Publikováno v:
BioMed Research International
BioMed Research International, Vol 2020 (2020)
BioMed Research International, Vol 2020 (2020)
The use of genetic testing to identify individuals with hereditary cancer syndromes has been widely adopted by clinicians for management of inherited cancer risk. The objective of this study was to develop and validate a 34-gene inherited cancer pred
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f81b27b0f9e58951a1ffb91b89096748
http://europepmc.org/articles/PMC6998746
http://europepmc.org/articles/PMC6998746
Akademický článek
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Autor:
Renius Owen, Yan Liu, Arlene Buller-Burckle, Sun Hee Rosenthal, Ke Zhang, Felicitas Lacbawan, Alla Smolgovsky
Publikováno v:
Cancer Research. 80:5741-5741
Background: Hereditary cancer accounts for 5% to 10% of all cancers. In addition to sequence variants, copy number variants (CNVs) are a cause of inherited cancer syndromes. Next-generation sequencing (NGS) technology enables simultaneous interrogati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d41f5222951f546c79b54e0fe54d467b
https://doi.org/10.1158/1538-7445.am2020-5741
https://doi.org/10.1158/1538-7445.am2020-5741
Autor:
Christina Bridges, Ramaswamy K. Iyer, Lisa V. Kalman, Pinar Bayrak-Toydemir, Jack Tarleton, Shannon D. Barker, Arlene Buller-Burckle, Lorraine Toji, Sherri J. Bale, Soma Das, Timothy D. Vo, Val V. Zvereff, Alan K. Percy, Swaroop Aradhya
Publikováno v:
The Journal of Molecular Diagnostics. 16(2):273-279
Rett syndrome is a dominant X-linked disorder caused by point mutations (approximately 80%) or by deletions or insertions (approximately 15% to 18%) in the MECP2 gene. It is most common in females but lethal in males, with a distinctly different phen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e315ac848c49892d05e21464ae541e4
Autor:
Zhao, Po1 (AUTHOR), Buller-Burckle, Arlene M.2 (AUTHOR) Arlene.M.Buller-Burkle@questdiagnositcs.com, Peng, Mei2 (AUTHOR), Anderson, Alison3 (AUTHOR), Han, Z. Jenny4 (AUTHOR), Gallivan, Monica V.E.4 (AUTHOR)
Publikováno v:
Hemoglobin. Feb2012, Vol. 36 Issue 1, p103-107. 5p.
Autor:
Mikula, M.1 mario.x.mikula@questdiagnostics.com, Buller-Burckle, A.1, Gallivan, M.2, Sun, W.1, Franklin, C. R.3, Strom, C. M.1
Publikováno v:
International Journal of Laboratory Hematology. Jun2011, Vol. 33 Issue 3, p310-317. 8p. 2 Diagrams, 3 Charts.