van Tuinen P - Search Results

1

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.

2

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.

3

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

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

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

7

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

8

Dyskeratosis congenita with linear areas of severe cutaneous involvement.

Baselga E, Drolet BA, van Tuinen P, Esterly NB, Happle R. Baselga E, et al. Among authors: van tuinen p. Am J Med Genet. 1998 Feb 17;75(5):492-6. Am J Med Genet. 1998. PMID: 9489792

9

The human multimerin gene MMRN maps to chromosome 4q22.

Torres MD, Van Tuinen P, Kroner PA. Torres MD, et al. Among authors: van tuinen p. Cytogenet Cell Genet. 2000;88(3-4):275-7. doi: 10.1159/000015537. Cytogenet Cell Genet. 2000. PMID: 10828608 No abstract available.

10

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

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