van Tuinen P - Search Results

1

Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia.

Heerema NA, Raimondi SC, Anderson JR, Biegel J, Camitta BM, Cooley LD, Gaynon PS, Hirsch B, Magenis RE, McGavran L, Patil S, Pettenati MJ, Pullen J, Rao K, Roulston D, Schneider NR, Shuster JJ, Sanger W, Sutcliffe MJ, van Tuinen P, Watson MS, Carroll AJ. Heerema NA, et al. Among authors: van tuinen p. Genes Chromosomes Cancer. 2007 Jul;46(7):684-93. doi: 10.1002/gcc.20451. Genes Chromosomes Cancer. 2007. PMID: 17431878 Free article.

2

Identification of High-risk Cryptic CRLF2 Rearrangements in B-Cell Acute Lymphoblastic Leukemia Utilizing an FGFR3/IGH Dual-Color Dual-Fusion DNA Probe Set.

Robin AJ, Peterson JF, Grignon JW Jr, Gheorghe G, Burke MJ, vanTuinen P. Robin AJ, et al. J Pediatr Hematol Oncol. 2017 May;39(4):e207-e210. doi: 10.1097/MPH.0000000000000691. J Pediatr Hematol Oncol. 2017. PMID: 27820126

3

Circulating Breast Carcinoma Cells Mimicking Therapy-Related Acute Myeloid Leukemia.

Rowan DJ, Logunova V, van Tuinen P, Olteanu H, Peterson JF. Rowan DJ, et al. Among authors: van tuinen p. Int J Surg Pathol. 2017 Feb;25(1):87-93. doi: 10.1177/1066896916664986. Epub 2016 Aug 20. Int J Surg Pathol. 2017. PMID: 27543510

4

The importance of communicating histories of gender assignment and reassignment to genetic laboratories.

Peterson JF, Andringa PJ, Grignon JW Jr, vanTuinen P. Peterson JF, et al. Genet Med. 2017 Nov;19(11):1205-1206. doi: 10.1038/gim.2017.44. Epub 2017 Apr 27. Genet Med. 2017. PMID: 28640245 Free article. No abstract available.

5

Inheritance of a Balanced t(12;20)(q24.33;p12.2) and Unbalanced der(13)t(7;13)(p21.3;q33.2) from a Maternally Derived Double Balanced Translocation Carrier.

Peterson JF, Geddes GC, Basel DG, Schippman D, Grignon JW Jr, vanTuinen P, Kappes UP. Peterson JF, et al. J Pediatr Genet. 2018 Mar;7(1):35-39. doi: 10.1055/s-0037-1605592. Epub 2017 Aug 14. J Pediatr Genet. 2018. PMID: 29441220 Free PMC article.

6

Elucidating discrepant results in a prenatal diagnosis of 48,XXY,+18 (Edwards and Klinefelter syndromes).

Peterson JF, Mikulec K, Grignon JW Jr, Behmaram B, Cruz MO, van Tuinen P. Peterson JF, et al. Among authors: van tuinen p. Am J Med Genet A. 2015 Nov;167A(11):2855-7. doi: 10.1002/ajmg.a.37250. Epub 2015 Jul 31. Am J Med Genet A. 2015. PMID: 26227211 No abstract available.

7

Concomitant 11p15.4-p15.5 duplication and terminal 22q13.33 deletion in a patient with features of Beckwith-Wiedemann syndrome.

Peterson JF, Bick DP, Geddes GC, McCarrier J, Grignon JW Jr, Chirempes B, Broeckel U, Abidi F, Rogers RC, Boccuto L, DuPont B, vanTuinen P. Peterson JF, et al. Am J Med Genet A. 2016 Dec;170(12):3348-3351. doi: 10.1002/ajmg.a.37939. Epub 2016 Aug 23. Am J Med Genet A. 2016. PMID: 27549580 No abstract available.

8

Mosaic Trisomy 9p in a Patient with Mild Dysmorphic Features and Normal Intelligence.

Brar R, Basel DG, Bick DP, Weik L, vanTuinen P, Peterson JF. Brar R, et al. J Assoc Genet Technol. 2017;43(2):56-58. J Assoc Genet Technol. 2017. PMID: 28511170

9

Proliferation centers in bone marrows involved by chronic lymphocytic leukemia/small lymphocytic lymphoma: a clinicopathologic analysis.

Chang JC, Harrington AM, Olteanu H, VanTuinen P, Kroft SH. Chang JC, et al. Ann Diagn Pathol. 2016 Dec;25:15-19. doi: 10.1016/j.anndiagpath.2016.07.011. Epub 2016 Aug 18. Ann Diagn Pathol. 2016. PMID: 27806839

10

Follicular lymphoma transformation to dual translocated Burkitt-like lymphoma: improved disease control associated with radiation therapy.

Parker SM, Olteanu H, VanTuinen P, Lawton CA, Schultz CJ, Christians KK, Fenske TS. Parker SM, et al. Int J Hematol. 2009 Dec;90(5):616-622. doi: 10.1007/s12185-009-0444-9. Epub 2009 Nov 25. Int J Hematol. 2009. PMID: 19937165

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