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Reha M. Toydemir

Oregon Health & Science University

12H指数
55论文数
1.2K被引数
收录论文 10
发表时间
Conventional Cytogenetic Analysis of Constitutional Abnormalities
err2024-06-05
err1
errOAAI
errBoles, Brittney; Gardner, Juli-Anne; Rehder, Catherine W.; Levy, Brynn; Velagaleti, Gopalrao V.; Toydemir, Reha M.; Sukov, William R.; Larson, Daniel P.; Cao, Yang; Mixon, Christopher; Vanderscheldon, Rachel K.; Zou, Ying S.; Astbury, Caroline; Tsuchiya, Karen D.; Peterson, Jess F.
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Conventional Cytogenetic Analysis of Hematologic Neoplasms A 20-Year Review of Proficiency Test Results From the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee
err2020-07-24
err4
errOAAI
errLarson, Daniel P.; Akkari, Yassmine M.; Van Dyke, Daniel L.; Raca, Gordana; Gardner, Juli-Anne; Rehder, Catherine W.; Kaiser-Rogers, Kathleen A.; Eagle, Penny; Yuhas, Jason A.; Gu, Jun; Toydemir, Reha M.; Kearney, Hutton; Conlin, Laura K.; Tang, Guilin; Dolan, Michelle M.; Ketterling, Rhett P.; Peterson, Jess F.
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Pediatric acute myeloid leukemia with t(7;21)(p22;q22)儿童急性髓系白血病伴t(7;21)(p22;q22)
err2019-02-14
err7
PREAI
errPaulraj, Prabakaran; Diamond, Steven; Razzaqi, Faisal; Ozeran, J. Daniel; Longhurst, Maria; Andersen, Erica F.; Toydemir, Reha M.; Hong, Bo
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Characterizing Atypical BCL6 Signal Patterns Detected by Digital Fluorescence In Situ Hybridization (FISH) Analysis
err2018-11-28
err1
errOAAI
errLiew, Michael; Rowe, Leslie R.; Szankasi, Phillipe; Paxton, Christian N.; Kelley, Todd; Toydemir, Reha M.; Salama, Mohamed E.
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A novel AGGF1-PDGFRβ fusion in pediatric T-cell acute lymphoblastic leukemia
err2017-12-28
err10
errOAAI
errZabriskie, Matthew S.; Antelope, Orlando; Verma, Anupam R.; Draper, Lauren R.; Eide, Christopher A.; Pomicter, Anthony D.; Thai Hoa Tran; Druker, Brian J.; Tyner, Jeffrey W.; Miles, Rodney R.; Graham, James M.; Hwang, Jae-Yeon; Varley, Katherine E.; Toydemir, Reha M.; Deininger, Michael W.; Raetz, Elizabeth A.; O'Hare, Thomas
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Developmental Delay and Colon Polyposis
err2017-10-01
err1
PREAI
errSamadder, N. Jewel; Burt, Randall W.; Toydemir, Reha M.
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Sheldon-Hall syndrome
err2009-03-23
err36
errOAAI
errToydemir, Reha M. }; Bamshad, Michael J.
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A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome
err2006-11-01
err129
errOAAI
errToydemir, Reha M.; Brassington, Anna E.; Bayrak-Toydemir, Pinar; Krakowiak, Patrycja A.; Jorde, Lynn B.; Whitby, Frank G.; Longo, Nicola; Viskochil, David H.; Carey, John C.; Bamshad, Michael J.
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Mutations in embryonic myosin heavy chain (MYH3) cause Freeman- Sheldon syndrome and Sheldon-Hall syndrome
err2006-04-16
err207
PREAI
errToydemir, RM; Rutherford, A; Whitby, FG; Jorde, LB; Carey, JC; Bamshad, MJ
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Expressivity of Holt-Oram syndrome is not predicted by TBX5 genotype
err2003-07-01
err103
errOAAI
errBrassington, AME; Sung, SS; Toydemir, RM; Le, T; Roeder, AD; Rutherford, AE; Whitby, FG; Jorde, LB; Bamshad, MJ
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