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1
Integration of high‐risk human papillomavirus into cellular cancer‐related genes in head and neck cancer cell lines
Integration of high‐risk human papillomavirus into cellular cancer‐related genes in head and neck cancer cell lines
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Integration of high‐risk human papillomavirus into cellular cancer‐related genes in head and neck cancer cell lines

Walline, Heather M. ; Goudsmit, Christine M. ; McHugh, Jonathan B. ; Tang, Alice L. ; Owen, John H. ; Teh, Bin T. ; McKean, Erin ; Glover, Thomas W. ; Graham, Martin P. ; Prince, Mark E. ; Chepeha, Douglas B. ; Chinn, Steven B. ; Ferris, Robert L. ; Gollin, Susanne M. ; Hoffmann, Thomas K. ; Bier, Henning ; Brakenhoff, Ruud ; Bradford, Carol R. ; Carey, Thomas E.

Head & neck, 2017-05, Vol.39 (5), p.840-852 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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2
Copy number variants are produced in response to low-dose ionizing radiation in cultured cells
Copy number variants are produced in response to low-dose ionizing radiation in cultured cells
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Copy number variants are produced in response to low-dose ionizing radiation in cultured cells

Arlt, Martin F. ; Rajendran, Sountharia ; Birkeland, Shanda R. ; Wilson, Thomas E. ; Glover, Thomas W.

Environmental and molecular mutagenesis, 2014-03, Vol.55 (2), p.103-113 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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3
A novel VEGFR3 mutation causes Milroy disease
A novel VEGFR3 mutation causes Milroy disease
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A novel VEGFR3 mutation causes Milroy disease

Butler, Matthew G. ; Dagenais, Susan L. ; Rockson, Stanley G. ; Glover, Thomas W.

American journal of medical genetics. Part A, 2007-06, Vol.143A (11), p.1212-1217 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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4
Effects of hydroxyurea on CNV induction in the mouse germline
Effects of hydroxyurea on CNV induction in the mouse germline
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Effects of hydroxyurea on CNV induction in the mouse germline

Arlt, Martin F. ; Rajendran, Sountharia ; Holmes, Sandra N. ; Wang, Kathleen ; Bergin, Ingrid L. ; Ahmed, Samreen ; Wilson, Thomas E. ; Glover, Thomas W.

Environmental and molecular mutagenesis, 2018-10, Vol.59 (8), p.698-714 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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5
9p partial monosomy and disorders of sex development: Review and postulation of a pathogenetic mechanism
9p partial monosomy and disorders of sex development: Review and postulation of a pathogenetic mechanism
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9p partial monosomy and disorders of sex development: Review and postulation of a pathogenetic mechanism

Quinonez, Shane C. ; Park, John M. ; Rabah, Raja ; Owens, Kailey M. ; Yashar, Beverly M. ; Glover, Thomas W. ; Keegan, Catherine E.

American journal of medical genetics. Part A, 2013-08, Vol.161A (8), p.1882-1896 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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6
Maternal intrachromosomal insertional translocation leads to recurrent 1q21.3q23.3 deletion in two siblings
Maternal intrachromosomal insertional translocation leads to recurrent 1q21.3q23.3 deletion in two siblings
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Maternal intrachromosomal insertional translocation leads to recurrent 1q21.3q23.3 deletion in two siblings

Quinonez, Shane C. ; Hedera, Peter ; Barr, Mason ; Ackley, Todd ; Lam, Cindy ; Purkayastha, Anjali ; Glover, Thomas W. ; Innis, Jeffrey W.

American journal of medical genetics. Part A, 2012-10, Vol.158A (10), p.2591-2601 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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7
Stably transfected common fragile site sequences exhibit instability at ectopic sites
Stably transfected common fragile site sequences exhibit instability at ectopic sites
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Stably transfected common fragile site sequences exhibit instability at ectopic sites

Ragland, Ryan L. ; Glynn, Michael W. ; Arlt, Martin F. ; Glover, Thomas W.

Genes chromosomes & cancer, 2008-10, Vol.47 (10), p.860-872 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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8
Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation
Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation
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Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation

Butler, Matthew G. ; Dagenais, Susan L. ; Garcia‐Perez, José L. ; Brouillard, Pascal ; Vikkula, Miikka ; Strouse, Peter ; Innis, Jeffrey W. ; Glover, Thomas W.

American journal of medical genetics. Part A, 2012-04, Vol.158A (4), p.839-849 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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9
Paracentric Inversion of Chromosome 21 Leading to Disruption of the HLCS Gene in a Family with Holocarboxylase Synthetase Deficiency
Paracentric Inversion of Chromosome 21 Leading to Disruption of the HLCS Gene in a Family with Holocarboxylase Synthetase Deficiency
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Paracentric Inversion of Chromosome 21 Leading to Disruption of the HLCS Gene in a Family with Holocarboxylase Synthetase Deficiency

Quinonez, Shane C. ; Seeley, Andrea H. ; Lam, Cindy ; Glover, Thomas W. ; Barshop, Bruce A. ; Keegan, Catherine E.

JIMD Reports, Volume 34, 2017-01, Vol.34, p.55-61 [Periódico revisado por pares]

Berlin, Heidelberg: Springer Berlin Heidelberg

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10
Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells
Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells
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Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells

Arlt, Martin F. ; Miller, Diane E. ; Beer, David G. ; Glover, Thomas W.

Genes chromosomes & cancer, 2002-01, Vol.33 (1), p.82-92 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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