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Items: 1 to 50 of 68

1.

Topical 2'-Hydroxyflavanone for Cutaneous Melanoma.

Bose C, Singh SP, Igid H, Green WC, Singhal SS, Lee J, Palade PT, Rajan A, Ball S, Tonk V, Hindle A, Tarbox M, Awasthi S.

Cancers (Basel). 2019 Oct 14;11(10). pii: E1556. doi: 10.3390/cancers11101556.

2.

A rare case of acute myeloid leukemia with der(1)t(1;19)(p13;p13.1).

McAlice M, Gohar M, Alshaban A, Orazi A, Tonk V, Chavali S, Tonk S, Gaur S.

Leuk Res Rep. 2019 Jun 8;12:100175. doi: 10.1016/j.lrr.2019.100175. eCollection 2019.

3.

Anticancer activity of 2'-hydroxyflavanone towards lung cancer.

Awasthi S, Singhal SS, Singhal J, Nagaprashantha L, Li H, Yuan YC, Liu Z, Berz D, Igid H, Green WC, Tijani L, Tonk V, Rajan A, Awasthi Y, Singh SP.

Oncotarget. 2018 Nov 16;9(90):36202-36219. doi: 10.18632/oncotarget.26329. eCollection 2018 Nov 16.

4.

Acute myeloid leukemia with KMT2A-SEPT5 translocation: A case report and review of the literature.

Elzamly S, Chavali S, Tonk V, Tonk S, Gaur S, Tarango D, Torabi A.

SAGE Open Med Case Rep. 2018 Jan 4;6:2050313X17750334. doi: 10.1177/2050313X17750334. eCollection 2018.

5.

Langerhans cell histiocytosis and diffuse large B-cell lymphoma with tetrasomy of PBX1 gene and t(14;19): two entities in one lymph node.

Moraveji S, Tonk V, Gaur S, Torabi A.

Pathology. 2016 Dec;48(7):728-731. doi: 10.1016/j.pathol.2016.07.016. Epub 2016 Oct 24. No abstract available.

PMID:
27788921
6.

Inaccuracy of non-invasive prenatal screening demands cautious counsel and follow-up.

Tonk VS, Wilson GN.

Am J Med Genet A. 2016 Apr;170A(4):1086-7. doi: 10.1002/ajmg.a.37530. Epub 2015 Dec 28. No abstract available.

PMID:
26708282
7.

Chromosome Xq13.2 Microduplication Involving an X-Inactivation Gene in a Girl with Short Stature, Madelung Deformity, and von Willebrand Disease.

Nur MM, Yamada M, Tonk V, Wilson GN.

J Pediatr Adolesc Gynecol. 2016 Apr;29(2):e39-42. doi: 10.1016/j.jpag.2015.11.010. Epub 2015 Nov 27.

PMID:
26639996
8.
9.

Complex/variant translocations in chronic myelogenous leukemia (CML): genesis and prognosis with 4 new cases.

Mendiola C, Ortega V, Tonk VS, Coviello JM, Velagaleti G.

Exp Mol Pathol. 2014 Aug;97(1):105-10. doi: 10.1016/j.yexmp.2014.06.004. Epub 2014 Jun 11.

PMID:
24927873
10.

Complete monosomy 21 confirmed by FISH and array-CGH.

Kulharya AS, Tonk VS, Lovell C, Flannery DB.

Am J Med Genet A. 2012 Apr;158A(4):935-7. doi: 10.1002/ajmg.a.35251. Epub 2012 Mar 9. No abstract available.

PMID:
22407893
11.

Interstitial deletion 5q14.3q21.3 with MEF2C haploinsufficiency and mild phenotype: when more is less.

Tonk V, Kyhm JH, Gibson CE, Wilson GN.

Am J Med Genet A. 2011 Jun;155A(6):1437-41. doi: 10.1002/ajmg.a.34012. Epub 2011 May 12.

PMID:
21567930
12.

Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia.

Wat MJ, Veenma D, Hogue J, Holder AM, Yu Z, Wat JJ, Hanchard N, Shchelochkov OA, Fernandes CJ, Johnson A, Lally KP, Slavotinek A, Danhaive O, Schaible T, Cheung SW, Rauen KA, Tonk VS, Tibboel D, de Klein A, Scott DA.

J Med Genet. 2011 May;48(5):299-307. doi: 10.1136/jmg.2011.089680.

13.

Fusion of HMGA2 to COG5 in uterine leiomyoma.

Velagaleti GV, Tonk VS, Hakim NM, Wang X, Zhang H, Erickson-Johnson MR, Medeiros F, Oliveira AM.

Cancer Genet Cytogenet. 2010 Oct 1;202(1):11-6. doi: 10.1016/j.cancergencyto.2010.06.002.

PMID:
20804914
14.

Juvenile myelomonocytic leukemia in a child with Crohn disease.

Oliver JW, Farnsworth B, Tonk VS.

Cancer Genet Cytogenet. 2006 May;167(1):70-3.

PMID:
16682290
15.

Correlation of abnormal rapid FISH and chromosome results from amniocytes for prenatal diagnosis.

Wyandt HE, Tonk VS, Huang XL, Evans AT, Milunsky JM, Milunsky A.

Fetal Diagn Ther. 2006;21(2):235-40.

PMID:
16491010
16.

Molecular cytogenetic characterization of a familial der(1)del(1)(p36.33)dup(1)(p36.33p36.22) with variable phenotype.

Tonk VS, Wilson GN, Yatsenko SA, Stankiewicz P, Lupski JR, Schutt RC, Northup JK, Velagaleti GV.

Am J Med Genet A. 2005 Dec 1;139A(2):136-40.

PMID:
16278888
17.

Costovertebral dysplasia in a patient with partial trisomy 22.

Tonk V, Wilson G, Schutt R, Mock J, Wyandt H, Mark HF, Ito M.

Exp Mol Pathol. 2006 Apr;80(2):197-200. Epub 2005 Nov 2.

PMID:
16259976
18.

Subtelomeric rearrangements in idiopathic mental retardation.

Velagaleti GV, Robinson SS, Rouse BM, Tonk VS, Lockhart LH.

Indian J Pediatr. 2005 Aug;72(8):679-85.

PMID:
16131774
19.

Prenatal diagnosis of FRA10A: a case report and literature review.

De Leon-Luis J, Santolaya-Forgas J, May G, Tonk V, Shelton D, Galan I.

Am J Med Genet A. 2005 Jul 1;136(1):63-5. Review.

PMID:
15937938
20.

FISH Variants with D15Z1.

Shim SH, Pan A, Huang XL, Tonk VS, Varma SK, Milunsky JM, Wyandt HE.

J Assoc Genet Technol. 2003;29(4):146-151.

PMID:
15213412
21.

Prenatal diagnosis of 47,XX,der(15)t(15;16)(q13;p13.2).

Santolaya-Forgas J, De Leon J, Powell WC, Tonk V.

Prenat Diagn. 2004 Mar;24(3):209-12.

PMID:
15057955
22.

Molecular cytogenetic characterization of a recombinant chromosome rec(22)dup(22q)inv(22)(p13q12.2).

Tonk VS, Jesurun CA, Morgan DL, Lockhart LH, Velagaleti GV.

Am J Med Genet A. 2004 Jan 1;124A(1):92-5.

PMID:
14679594
23.

Familial interstitial deletion of chromosome 4 (p15.2p16.1).

Tonk VS, Jalal SM, Gonzalez J, Kennedy A, Velagaleti GV.

Ann Genet. 2003 Oct-Dec;46(4):453-8.

PMID:
14659781
24.

Aberrant methylation of the cyclin D2 promoter in primary small cell, nonsmall cell lung and breast cancers.

Virmani A, Rathi A, Heda S, Sugio K, Lewis C, Tonk V, Takahashi T, Roth JA, Minna JD, Euhus DM, Gazdar AF.

Int J Cancer. 2003 Nov 10;107(3):341-5.

25.

Disease associated balanced chromosome rearrangements (DBCR): report of two new cases.

Tonk VS, Wyandt HE, Huang X, Patel N, Morgan DL, Kukolich M, Lockhart LH, Velagaleti GV.

Ann Genet. 2003 Jan-Mar;46(1):37-43.

PMID:
12818528
26.

Aberrant methylation of TMS1 in small cell, non small cell lung cancer and breast cancer.

Virmani A, Rathi A, Sugio K, Sathyanarayana UG, Toyooka S, Kischel FC, Tonk V, Padar A, Takahashi T, Roth JA, Euhus DM, Minna JD, Gazdar AF.

Int J Cancer. 2003 Aug 20;106(2):198-204.

27.

De novo supernumerary ring chromosome 7: first report of a non-mosaic patient and review of the literature.

Velagaleti GV, Jalal SM, Kukolich MK, Lockhart LH, Tonk VS.

Clin Genet. 2002 Mar;61(3):202-6. Review.

PMID:
12000362
28.

Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay.

Levy B, Jalal SM, Dunn TM, Warburton PE, Tonk VS, Hirschhorn K, Lockhart LH, Hughes T, Velagaleti GV.

Am J Med Genet. 2002 Mar 15;108(3):198-204.

PMID:
11891685
29.

Interstitial deletion of 20q in a patient with Waldenström macroglobulinemia following chemotherapy.

Blann MM, Velagaleti GV, Morgan DL, Martinez RE, Conlin PA, Tonk VS.

Cancer Genet Cytogenet. 2002 Jan 15;132(2):145-8.

PMID:
11850077
30.

Maternal complex chromosome rearrangement ascertained through a del (13)(q12.1q14.1) detected in her mildly affected daughter.

Drummond-Borg M, Kulharya AS, Tonk V, Garcia-Heras J.

Am J Med Genet. 2002 Jan 1;107(1):61-3.

PMID:
11807870
31.

Duplication 8 [inv dup(8)(p12p23)] with macrocephaly.

Tonk VS, Wilson GN, Velagaleti GV.

Ann Genet. 2001 Oct-Dec;44(4):195-9.

PMID:
11755105
32.

Trisomy 5p. A case report and review.

Velagaleti GV, Morgan DL, Tonk VS.

Ann Genet. 2000 Jul-Dec;43(3-4):143-5. Review.

PMID:
11164196
33.

Duplication of 1q in a child with down syndrome and myelodysplastic syndrome.

Blann MM, Morgan DL, Oblender M, Heinen B, Williams J, Tonk VS.

Cancer Genet Cytogenet. 2000 May;119(1):74-6.

PMID:
10812176
34.

Constitutional (5;18) in a patient with aplastic anemia.

Keung YK, Suwanvecho S, Cobos E, Tonk V.

Cancer Genet Cytogenet. 1999 Jul 15;112(2):184-5. No abstract available.

PMID:
10686951
35.

Ring chromosome 8 syndrome: further characterization.

Tonk VS, Kukolich MK, Morgan D, Khan A, Jalal SM.

Am J Med Genet. 2000 Jan 17;90(2):162-4.

PMID:
10607957
36.

Retinal pigment mosaicism in Pallister-Killian syndrome (mosaic tetrasomy 12p).

Graham W, Brown SM, Shah F, Tonk VS, Kukolich MK.

Arch Ophthalmol. 1999 Dec;117(12):1648-9. No abstract available.

PMID:
10604674
37.

"Jumping translocation" and multiple myeloma.

Keung YK, Balogun OA, Tonk V.

Cancer Genet Cytogenet. 1999 Jul 1;112(1):60-1. No abstract available.

PMID:
10432939
38.

Two distinct forms of the 64,000 Mr protein of the cleavage stimulation factor are expressed in mouse male germ cells.

Wallace AM, Dass B, Ravnik SE, Tonk V, Jenkins NA, Gilbert DJ, Copeland NG, MacDonald CC.

Proc Natl Acad Sci U S A. 1999 Jun 8;96(12):6763-8.

39.
40.

Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.

Zinn AR, Tonk VS, Chen Z, Flejter WL, Gardner HA, Guerra R, Kushner H, Schwartz S, Sybert VP, Van Dyke DL, Ross JL.

Am J Hum Genet. 1998 Dec;63(6):1757-66.

41.

Characterization of paired tumor and non-tumor cell lines established from patients with breast cancer.

Gazdar AF, Kurvari V, Virmani A, Gollahon L, Sakaguchi M, Westerfield M, Kodagoda D, Stasny V, Cunningham HT, Wistuba II, Tomlinson G, Tonk V, Ashfaq R, Leitch AM, Minna JD, Shay JW.

Int J Cancer. 1998 Dec 9;78(6):766-74.

42.

Unusual presentation of multiple myeloma with "jumping translocation" involving 1q21. A case report and review of the literature.

Keung YK, Yung C, Wong JW, Shah F, Cobos E, Tonk V.

Cancer Genet Cytogenet. 1998 Oct 15;106(2):135-9. Review.

PMID:
9797778
43.

Translocation (1;22) in refractory anemia and the prognostic significance of karyotypic abnormalities in refractory anemia.

Keung YK, Cobos E, Tonk V, Morgan D.

Cancer Genet Cytogenet. 1998 Oct 1;106(1):72-5. Review.

PMID:
9772913
44.

Characterization of a breast cancer cell line derived from a germ-line BRCA1 mutation carrier.

Tomlinson GE, Chen TT, Stastny VA, Virmani AK, Spillman MA, Tonk V, Blum JL, Schneider NR, Wistuba II, Shay JW, Minna JD, Gazdar AF.

Cancer Res. 1998 Aug 1;58(15):3237-42.

45.

Comparison between fluorescence in situ hybridization and classical cytogenetics in human tumors.

Virmani AK, Tonk VS, Gazdar AF.

Anticancer Res. 1998 May-Jun;18(3A):1351-6.

PMID:
9673339
46.

Allelotyping demonstrates common and distinct patterns of chromosomal loss in human lung cancer types.

Virmani AK, Fong KM, Kodagoda D, McIntire D, Hung J, Tonk V, Minna JD, Gazdar AF.

Genes Chromosomes Cancer. 1998 Apr;21(4):308-19.

PMID:
9559342
47.

Del (X)(p21.2) in a mother and two daughters with variable ovarian function.

Zinn AR, Ouyang B, Ross JL, Varma S, Bourgeois M, Tonk V.

Clin Genet. 1997 Oct;52(4):235-9.

PMID:
9383030
48.

Double minute chromosomes and myelodysplastic syndrome: a case report and literature review.

Keung YK, Cobos E, Morgan D, Whitehead RP, Tonk V.

Cancer Genet Cytogenet. 1997 Sep;97(2):94-6. Review.

PMID:
9283588
49.

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