V. Tonk

发表

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

M. Westerfield, J. Minna, I. Wistuba, 1998, International journal of cancer.

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

V. Tonk, C. Mendiola, V. Ortega, 2014, Experimental and molecular pathology.

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

J. Minna, S. Toyooka, J. Roth, 2003, International journal of cancer.

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

N. Copeland, D. Gilbert, N. Jenkins, 1999, Proceedings of the National Academy of Sciences of the United States of America.

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

A. Zinn, V. Tonk, M. Bourgeois, 1997, Clinical genetics.

Renal cell carcinoma with translocation (X;1). Further evidence for a cytogenetically defined subtype.

V. Tonk, C. Timmons, G. Tomlinson, 1995, Cancer genetics and cytogenetics.

Topical 2′-Hydroxyflavanone for Cutaneous Melanoma

V. Tonk, Jihyun Lee, S. Awasthi, 2019, Cancers.

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

Golder N Wilson, P. Stankiewicz, J. Lupski, 2005, American journal of medical genetics. Part A.

Chromosomal localization of a human mucin gene (MUC8) and cloning of the cDNA corresponding to the carboxy terminus.

N. Nowak, R. Eddy, T. Shows, 1997, American journal of respiratory cell and molecular biology.

Complement Gene Mutation and Ehlers-Danlos Syndrome

V. Tonk, G. Wilson, S. Tonk, 2020, Journal of Biosciences and Medicines.

Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences

R. W. Huff, J. Wiszniewska, E. Roeder, 2022, Journal of Medical Genetics.

Juvenile myelomonocytic leukemia in a child with Crohn disease.

V. Tonk, J. Oliver, Brent Farnsworth, 2006, Cancer genetics and cytogenetics.

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

V. Tonk, Y. Keung, E. Cobos, 1998, Cancer genetics and cytogenetics.

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

V. Tonk, Y. Keung, R. Whitehead, 1997, Cancer genetics and cytogenetics.

Rhabdoid tumor of the kidney with primitive neuroectodermal tumor of the central nervous system: Associated tumors with different histologic, cytogenetic, and molecular findings

V. Tonk, C. Timmons, G. Tomlinson, 1994, Genes, chromosomes & cancer.

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

V. Tonk, S. Elzamly, S. Gaur, 2018, SAGE open medical case reports.

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

V. Tonk, D. Morgan, H. Wyandt, 2003, Annales de genetique.

Trisomy 5p. A case report and review.

V. Tonk, D. Morgan, G. Velagaleti, 2000, Annales de genetique.

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

V. Tonk, Y. Keung, J. Wong, 1998, Cancer genetics and cytogenetics.

Interstitial deletions 4q21.1q25 and 4q25q27: phenotypic variability and relation to Rieger anomaly.

Golder N Wilson, V. Tonk, N. Schneider, 1995, American journal of medical genetics.

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

V. Tonk, G. Velagaleti, S. Jalal, 2003, Annales de genetique.

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

S. Schwartz, A. Zinn, V. Tonk, 1998, American journal of human genetics.

A CNV Catalogue

Golder N Wilson, V. Tonk, H. Wyandt, 2017 .

Fusion of HMGA2 to COG5 in uterine leiomyoma.

V. Tonk, F. Medeiros, André M. Oliveira, 2010, Cancer genetics and cytogenetics.

Costovertebral dysplasia in a patient with partial trisomy 22.

V. Tonk, Masamichi Ito, H. Wyandt, 2006, Experimental and molecular pathology.

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

V. Tonk, A. Kulharya, M. Drummond-Borg, 2002, American journal of medical genetics.

Cytogenetic and molecular cytogenetic studies of a case of interstitial deletion of proximal 15q

V. Tonk, B. Wu, B. Haddad, 1995, Clinical genetics.

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

Arvind Virmani, John D Minna, Jack A Roth, 2003, International journal of cancer.

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

V. Tonk, S. Gaur, S. Moraveji, 2016, Pathology.

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

J. Minna, A. Gazdar, I. Wistuba, 1998, Cancer research.

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

Anthony Johnson, Daryl A Scott, Thomas Schaible, 2011, Journal of Medical Genetics.

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

V. Tonk, G. Velagaleti, G. Wilson, 2001, Annales de genetique.

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

V. Tonk, D. Morgan, G. Velagaleti, 2004, American journal of medical genetics. Part A.

Advances in Brief Characterization of a Breast Cancer Cell Line Derived from a GermLine BRCA 1 Mutation Carrier 1

Arvind, Joanne, Monique, 1998 .

Chromosomal alterations of pediatric malignancy in a West Texas population

V. Tonk, S. Awasthi, C. Bose, 2020 .

Array-Comparative Genomic Hybridization/Microarray Analysis: Interpretation of Copy Number Variants

Golder N Wilson, V. Tonk, H. Wyandt, 2017 .

Analyzing the most frequent disease loci in targeted patient categories optimizes disease gene identification and test accuracy worldwide

V. Tonk, R. Lebo, 2015, Journal of Translational Medicine.

Copy Number Variants

V. Tonk, H. Wyandt, 2011 .

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

J. Minna, A. Gazdar, A. Virmani, 1998, Genes, chromosomes & cancer.

Relapse of precursor B-cell acute lymphoblastic leukemia as an isolated central nervous system mass lesion 9 years after initial diagnosis.

V. Tonk, C. Timmons, N. Winick, 1996, Medical and pediatric oncology.

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

V. Tonk, D. Morgan, M. Blann, 2000, Cancer genetics and cytogenetics.

Robertsonian (15q;15q) translocation in a child with Angelman syndrome: evidence of uniparental disomy.

Golder N Wilson, D. Ledbetter, S. Christian, 1996, American journal of medical genetics.

Chromosome Heteromorphism (Summaries)

Golder N Wilson, V. Tonk, H. Wyandt, 2017 .

Prenatal diagnosis of FRA10A: A case report and literature review

V. Tonk, J. Santolaya-Forgas, J. León-Luis, 2005, American journal of medical genetics. Part A.

Identification and molecular confirmation of a small chromosome 10q duplication [dir dup(10)(q24.2-->q24.3)] inherited from a mother mosaic for the abnormality.

N R Schneider, V. Tonk, M. Delgado, 1996, American journal of medical genetics.

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

V. Tonk, A. Orazi, S. Gaur, 2019, Leukemia research reports.

Gene and Genome Sequencing: Interpreting Genetic Variation at the Nucleotide Level

Golder N Wilson, V. Tonk, H. Wyandt, 2017 .

Deletion of 15q12 in Angelman syndrome: report of 3 new cases

V. Tonk, H. Wyandt, A. Milunsky, 1992, Clinical genetics.

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

Golder N Wilson, V. Tonk, G. Wilson, 2016, Journal of pediatric and adolescent gynecology.

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

V. Tonk, M. Kukolich, S. M. Brown, 1999, Archives of ophthalmology.

Methods of Studying Human Chromosomes and Nomenclature. The Normal Human Karyotype

V. Tonk, G. Velagaleti, 2004 .

Chromosome Variation Detected by Fluorescent In Situ Hybridization (FISH)

Golder N Wilson, V. Tonk, H. Wyandt, 2017 .

7 FISH Technologies

V. Tonk, H. Wyandt, 2004 .

Report of a complex karyotype in recurrent metastatic fibrolamellar hepatocellular carcinoma and a review of hepatocellular carcinoma cytogenetics.

V. Tonk, C. Timmons, M. Ansari, 1996, Cancer genetics and cytogenetics.

Interphase cytogenetic (in situ hybridization) analysis of astrocytomas using archival, formalin-fixed, paraffin-embedded tissue and nonfluorescent light microscopy.

V. Tonk, C. White, A. Perry, 1997, American journal of clinical pathology.

Trisomy 2, trisomy 20, and del(17p) as sole chromosomal abnormalities in three cases of hepatoblastoma

V. Tonk, C. Timmons, N. Schneider, 1994, Genes, chromosomes & cancer.

Moving towards a syndrome: a review of 20 cases and a new case of non‐mosaic tetrasomy 9p with long‐term survival

V. Tonk, 1997, Clinical genetics.

Atlas of Human Chromosome Heteromorphisms

V. Tonk, H. Wyandt, 2004, Springer Netherlands.

Subtelomeric rearrangements in idiopathic mental retardation

V. Tonk, G. Velagaleti, B. Rouse, 2005, Indian journal of pediatrics.

Translocation t(15;17) in acute myelogenous leukemia with atypical megakaryoblastic features: diagnostic, clinical, and therapeutic implications.

V. Tonk, T. McConnell, D. Morgan, 1996, Cancer genetics and cytogenetics.

Human Chromosome Variation: Heteromorphism and Polymorphism

V. Tonk, H. Wyandt, 2011, Springer Netherlands.

A report of a rare chromosome 9 variant with an unusual G-banding pattern in the 9qh region

V. Tonk, J. Krishna, 1997, Indian Journal of Pediatrics.

Normal Population Studies

V. Tonk, H. Wyandt, 2004 .

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

Golder N Wilson, V. Tonk, G. Wilson, 2011, American journal of medical genetics. Part A.

Interstitial deletion of long arm of chromosome no. 5 with growth hormone deficiency‐an emerging syndrome?

V. Tonk, J. Krishna, M. Bourgeois, 1997, Clinical genetics.

Ring chromosome 8 syndrome: further characterization.

V. Tonk, D. Morgan, S. Jalal, 2000, American journal of medical genetics.

Case report: denovo inherited 18p deletion in a mother-fetus pair with extremely variable expression, confirmed by fluorescence in situ hybridization (FISH) analysis.

V. Tonk, J. Krishna, 1997, European journal of obstetrics, gynecology, and reproductive biology.

Development of minimally differentiated acute myeloblastic leukemia with novel isochromosome 18p and antecedent aplastic anemia.

V. Tonk, Y. Keung, E. Cobos, 1996, Cancer genetics and cytogenetics.

Anticancer activity of 2’-hydroxyflavanone towards lung cancer

Yate-Ching Yuan, V. Tonk, Y. Awasthi, 2018, Oncotarget.

Do Severe Complications Like Aneurysms from Kawasaki and Kawasaki-Like Infections Arise in Children with Underlying Articulo-Autonomic Dysplasia/Ehlers-Danlos Syndrome?

V. Tonk, G. Wilson, 2020 .

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

K. Hirschhorn, V. Tonk, P. Warburton, 2002, American journal of medical genetics.

Chronic eosinophilic leukemia and hypereosinophilic syndromes. Proposal for classification, literature review, and report of a case with a unique chromosomal abnormality.

V. Tonk, D. Morgan, J. Oliver, 1998, Cancer genetics and cytogenetics.

Correlation of Abnormal Rapid FISH and Chromosome Results from Amniocytes for Prenatal Diagnosis

J. Milunsky, V. Tonk, H. Wyandt, 2006, Fetal Diagnosis and Therapy.

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

V. Tonk, D. Morgan, G. Velagaleti, 2002, Cancer genetics and cytogenetics.

Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis

Golder N Wilson, V. Tonk, H. Wyandt, 2017 .

Complete monosomy 21 confirmed by FISH and array‐CGH

V. Tonk, D. Flannery, A. Kulharya, 2012, American journal of medical genetics. Part A.

Mitochondrial Dysfunction Contributes to Ehlers-Danlos Syndrome - A Patient Presentation

Golder N Wilson, V. Tonk, 2020 .

Genetics and Dysmorphology

Golder N Wilson, V. Tonk, O. Naga, 2015 .

Genetic Disorders

Golder N Wilson, V. Tonk, O. Naga, 2019, Pediatric Board Study Guide.

Is Array-Comparative Genomic Hybridization Useful for Children with Apparently Isolated Congenital Anomalies?

Golder N Wilson, V. Tonk, 2018 .