Toydemir RM - Search Results

1

Pediatric acute myeloid leukemia with t(7;21)(p22;q22).

Paulraj P, Diamond S, Razzaqi F, Ozeran JD, Longhurst M, Andersen EF, Toydemir RM, Hong B. Paulraj P, et al. Among authors: toydemir rm. Genes Chromosomes Cancer. 2019 Aug;58(8):551-557. doi: 10.1002/gcc.22740. Epub 2019 Feb 14. Genes Chromosomes Cancer. 2019. PMID: 30706625 Review.

2

Chronic myelomonocytic leukemia with ETV6-ABL1 rearrangement and SMC1A mutation.

Cessna MH, Paulraj P, Hilton B, Sadre-Bazzaz K, Szankasi P, Cluff A, Patel JL, Hoda D, Toydemir RM. Cessna MH, et al. Among authors: toydemir rm. Cancer Genet. 2019 Oct;238:31-36. doi: 10.1016/j.cancergen.2019.07.004. Epub 2019 Jul 13. Cancer Genet. 2019. PMID: 31425923

3

Flow Cytometry Is More Sensitive Than Fluorescence In Situ Hybridization for Detecting Minimal Residual Disease.

Ng DP, Miles RR, Andersen EF, Toydemir RM. Ng DP, et al. Among authors: toydemir rm. Am J Clin Pathol. 2021 Sep 8;156(4):715-716. doi: 10.1093/ajcp/aqab080. Am J Clin Pathol. 2021. PMID: 34165497 No abstract available.

4

Clinical features of trisomy 12 mosaicism-Report and review.

Hong B, Zunich J, Openshaw A, Toydemir RM. Hong B, et al. Among authors: toydemir rm. Am J Med Genet A. 2017 Jun;173(6):1681-1686. doi: 10.1002/ajmg.a.38194. Epub 2017 Mar 27. Am J Med Genet A. 2017. PMID: 28345774

5

Detection of genome-wide copy number variants in myeloid malignancies using next-generation sequencing.

Shen W, Paxton CN, Szankasi P, Longhurst M, Schumacher JA, Frizzell KA, Sorrells SM, Clayton AL, Jattani RP, Patel JL, Toydemir R, Kelley TW, Xu X. Shen W, et al. J Clin Pathol. 2018 Apr;71(4):372-378. doi: 10.1136/jclinpath-2017-204823. Epub 2017 Dec 2. J Clin Pathol. 2018. PMID: 29197855

6

Seizures and Cardiomyopathy in a Patient with Pallister-Killian Syndrome due to Hexasomy 12p Mosaicism.

Toydemir RM, Panza E, Longhurst MC, South ST, Rope AF. Toydemir RM, et al. Mol Syndromol. 2020 Jul;11(3):125-129. doi: 10.1159/000507598. Epub 2020 Apr 10. Mol Syndromol. 2020. PMID: 32903844 Free PMC article.

7

Multiple Congenital Anomalies and Global Developmental Delay in a Patient with Interstitial 6q25.2q26 Deletion: A Diagnostic Odyssey.

Paulraj P, Palumbos JC, Openshaw A, Carey JC, Toydemir RM. Paulraj P, et al. Among authors: toydemir rm. Cytogenet Genome Res. 2018;156(4):191-196. doi: 10.1159/000494871. Epub 2018 Nov 16. Cytogenet Genome Res. 2018. PMID: 30439704

8

Genome-wide uniparental disomy as a mechanism of immune escape in acquired aplastic anaemia.

Tantravahi SK, Huber BD, Vagher J, Maese L, Pomicter AD, Al-Sweel N, Asch JD, Toydemir RM, Hong B, Parker C. Tantravahi SK, et al. Among authors: toydemir rm. Br J Haematol. 2022 Sep;198(6):e78-e81. doi: 10.1111/bjh.18351. Epub 2022 Jul 25. Br J Haematol. 2022. PMID: 35876645 No abstract available.

9

Delineation of the 9q31 deletion syndrome: Genomic microarray characterization of two patients with overlapping deletions.

Dugan SL, Panza E, Openshaw A, Botto LD, Camacho JA, Toydemir RM. Dugan SL, et al. Among authors: toydemir rm. Am J Med Genet A. 2018 Dec;176(12):2901-2906. doi: 10.1002/ajmg.a.40664. Epub 2018 Oct 22. Am J Med Genet A. 2018. PMID: 30346094

10

Identification of KMT2A-ARHGEF12 fusion in a child with a high-grade B-cell lymphoma.

Schafernak KT, Williams JA, Clyde BI, Marcus C, Decker B, Toydemir RM. Schafernak KT, et al. Among authors: toydemir rm. Cancer Genet. 2021 Nov;258-259:23-26. doi: 10.1016/j.cancergen.2021.06.006. Epub 2021 Jun 27. Cancer Genet. 2021. PMID: 34237703

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