Zobrazeno 1 - 10
of 222
pro vyhledávání: '"Warren G, Sanger"'
Autor:
Bhavana J. Dave, Wing C. Chan, Kai Fu, Oskar Hagberg, Carsten Wiuf, Lynette Smith, Warren G. Sanger, Michelle M. Hess, Li Xiao, Ken Young, Huimin Geng, Javeed Iqbal, Eric Chan, Francesco d'Amore
Supplementary Data from Clonal Evolution in t(14;18)-Positive Follicular Lymphoma, Evidence for Multiple Common Pathways, and Frequent Parallel Clonal Evolution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::176d88875abb809f44989c6a14d73a9e
https://doi.org/10.1158/1078-0432.22439284.v1
https://doi.org/10.1158/1078-0432.22439284.v1
Autor:
Bhavana J. Dave, Wing C. Chan, Kai Fu, Oskar Hagberg, Carsten Wiuf, Lynette Smith, Warren G. Sanger, Michelle M. Hess, Li Xiao, Ken Young, Huimin Geng, Javeed Iqbal, Eric Chan, Francesco d'Amore
Purpose: Follicular lymphoma typically has acquired a t(14;18) translocation, but subsequent additional cytogenetic abnormalities contribute to disease progression. The main aims of the study are to (a) identify the frequency and temporal sequence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3211182039d2e10555477f96f3f1bc30
https://doi.org/10.1158/1078-0432.c.6516778.v1
https://doi.org/10.1158/1078-0432.c.6516778.v1
Autor:
Ji Yuan, Stephanie P. Mathews, Kathleen W. Rao, Nathan D. Montgomery, Wilborn B. Coward, Steven M Johnson, Jennifer N. Sanmann, Warren G. Sanger, Margaret L. Gulley, Kathleen Kaiser-Rogers, Yuri Fedoriw
Publikováno v:
Cancer Genetics. 209:408-416
Classical Hodgkin lymphoma (CHL) is morphologically characterized by scattered malignant Hodgkin/Reed-Sternberg (HRS) cells that are far outnumbered by surrounding reactive hematolymphoid cells. Approximately half of all cases of CHL are associated w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3a01477dd095846ad466f31f5f2494f
https://doi.org/10.1016/j.cancergen.2016.08.006
https://doi.org/10.1016/j.cancergen.2016.08.006
Publikováno v:
Genetics in Medicine. 18:643-648
These ACMG standards and guidelines are developed primarily as an educational resource for clinical laboratory geneticists to help them provide quality clinical laboratory genetic services. Adherence to these standards and guidelines is voluntary and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ef33508737487acc323fc162854e078
https://doi.org/10.1038/gim.2016.51
https://doi.org/10.1038/gim.2016.51
Autor:
Bret C. Mobley, Murat Gokden, Warren G. Sanger, Hilary Highfield Nickols, Marilu Nelson, Lola B. Chambless, Manoj Kumar
Publikováno v:
Human Pathology. 46:1232-1236
Papillary tumor of the pineal region (PTPR) is an uncommon neoplasm with variable biologic behavior. Cytogenetic and molecular diagnostic studies are rare, yielding no definitive genetic signature. We report a case of PTPR with a multicentric present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a48f4cc5f2326811040526095078fe6
https://doi.org/10.1016/j.humpath.2015.04.014
https://doi.org/10.1016/j.humpath.2015.04.014
Autor:
Christopher W. Bartlett, Tiffany P. Hogan, Jenya Iuzzini-Seigel, Tracy M. Centanni, Warren G. Sanger, Jordan R. Green, J. N. Sanmann
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 168:536-543
Childhood apraxia of speech (CAS) is a debilitating pediatric speech disorder characterized by varying symptom profiles, comorbid deficits, and limited response to intervention. Specific Language Impairment (SLI) is an inherited pediatric language di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49ca4f8d2b9495699402a51dc8d9dcf5
https://doi.org/10.1002/ajmg.b.32325
https://doi.org/10.1002/ajmg.b.32325
Autor:
Melissa Agsalda-Garcia, Warren G. Sanger, Thomas G. Gross, James R. Anderson, Lara Mussolin, Paul J. Galardy, Bruce Shiramizu, Matthew J. Barth, Sherrie L. Perkins, Lauren Harrison, J. Kimble Frazer, Lynette M. Smith, Mitchell S. Cairo, Stanton Goldman, Howard J. Weinstein
Publikováno v:
British Journal of Haematology. 170:367-371
Patient-specific primers from 10 children/adolescents with Burkitt leukaemia (BL) ± central nervous system disease who were treated with French-British-American/Lymphome Malins de Burkitt 96 C1 plus rituximab were developed from diagnostic blood/bon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dcad695c75525a401660137eeb9dcbe
https://doi.org/10.1111/bjh.13443
https://doi.org/10.1111/bjh.13443
Publikováno v:
Cytogenetic and Genome Research. 147:31-34
Sex chromosome aneuploidies range in incidence from rather common to exceedingly rare and have a variable phenotype. We report 2 patients with sex chromosome aneuploidies who developed severe aplastic anemia requiring treatment. The first patient had
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::082d528fc51b5b23375c3c68a6f8e1e6
https://doi.org/10.1159/000441585
https://doi.org/10.1159/000441585
Autor:
Warren G. Sanger, Bhavana J. Dave
Publikováno v:
The AGT Cytogenetics Laboratory Manual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::751accd8455e2aea0556afa98c81428d
https://doi.org/10.1002/9781119061199.ch18
https://doi.org/10.1002/9781119061199.ch18
Autor:
Peter F. Coccia, Phyllis I. Warkentin, Warren G. Sanger, James L. Wisecarver, Sachit Patel, James Harper, Bruce Geoffrey Gordon, Don W. Coulter, Alfred C. Grovas
Publikováno v:
Journal of Pediatric Hematology/Oncology
Juvenile myelomonocytic leukemia (JMML) is a rare mixed myelodysplastic and myeloproliferative clonal disorder of early childhood representing about 1% to 2% of all pediatric leukemias.1–3 Most cases present before 6 years of age, with a median age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc4781b047116ae5f4cba4fea974f80e
https://doi.org/10.1097/mph.0000000000000077
https://doi.org/10.1097/mph.0000000000000077