T. Glover

M. W. Glynn, T. Glover, C. Downs, 2003, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

A translocation interrupts the COL5A1 gene in a patient with Ehlers–Danlos syndrome and hypomelanosis of Ito

P. Byers, T. Glover, D. Greenspan, 1996, Nature Genetics.

Characterization of human homologs of the Drosophila seven in absentia (sina) gene.

A. Look, E. Fearon, T. Glover, 1997, Genomics.

An FHIT tumor suppressor gene?

M. L. Le Beau, T. Glover, David I. Smith, 1998, Genes, chromosomes & cancer.

Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSAS.

P. Marynen, J. Fryns, T. Glover, 1995, Journal of medical genetics.

SHORT COMMUNICATION /WI-Related Locus on Chromosome 15

F. Collins, T. Glover, M. Wallace, 1992 .

NF1-related locus on chromosome 15.

F. Collins, T. Glover, M. Wallace, 1992, Genomics.

Molecular and cytogenetic analysis of tumors in von recklinghausen neurofibromatosis

T. Glover, L. B. Andersen, E. Legius, 1991, Genes, chromosomes & cancer.

Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome 3 in an esophageal adenocarcinoma

D. Beer, T. Glover, M. Arlt, 2001, Genes, chromosomes & cancer.

Comparison of Constitutional and Replication Stress-Induced Genome Structural Variation by SNP Array and Mate-Pair Sequencing

T. E. Wilson, T. Glover, R. Lyons, 2011, Genetics.

Ultraviolet light induction of diphtheria toxin-resistant mutants of normal and xeroderma pigmentosum human fibroblasts.

J. Trosko, Chia‐cheng Chang, T. Glover, 1979, Proceedings of the National Academy of Sciences of the United States of America.

A phosphoglycerate mutase brain isoform (PGAM 1) pseudogene is localized within the human Menkes disease gene (ATP7 A).

T. Glover, J. Mercer, H. Dierick, 1997, Gene.

X-linked mental retardation: a study of 7 families.

P. Jacobs, T. Glover, H. G. Dunn, 1980, American journal of medical genetics.

Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndrome.

T. Glover, R. Erickson, M. Witte, 2004, Gene expression patterns : GEP.

Comparative Study of X-Ray and UV Induced Cytotoxicity, DNA Repair, and Mutagenesis in Down's Syndrome and Normal Fibroblasts

J. Trosko, T. Glover, D. Segal, 1980, Pediatric Research.

svCapture: efficient and specific detection of very low frequency structural variant junctions by error-minimized capture sequencing

T. E. Wilson, T. Glover, J. Salk, 2022, bioRxiv.

The murine Fhit gene is highly similar to its human orthologue and maps to a common fragile site region.

D. Beer, T. Glover, H. Dierick, 1998, Cancer research.

Precise localization of aphidicolin-induced breakpoints on the short arm of human chromosome 3.

T. Glover, D. Smith, B. Opalka, 1995, Genomics.

Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma.

T. Glover, R. Gemmill, H. Drabkin, 1994, Genomics.

Positional cloning of the hereditary renal carcinoma 3;8 chromosome translocation breakpoint.

T. Glover, F. Li, R. Gemmill, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes.

F. Hecht, T. Glover, F. Li, 1988, Cancer genetics and cytogenetics.

Effects of hydroxyurea on CNV induction in the mouse germline

T. E. Wilson, T. Glover, I. Bergin, 2018, Environmental and molecular mutagenesis.

Differential Roles for DNA Polymerases Eta, Zeta, and REV1 in Lesion Bypass of Intrastrand versus Interstrand DNA Cross-Links

T. Glover, C. Canman, M. Paulsen, 2009, Molecular and Cellular Biology.

Human Na+- myo-inositol cotransporter gene: alternate splicing generates diverse transcripts.

T. Glover, M. Togawa, F. Porcellati, 1998, American journal of physiology. Cell physiology.

Localization of DNA sequences to a region within Xp11.21 between incontinentia pigmenti (IP1) X-chromosomal translocation breakpoints.

T. Glover, E. Burright, E. Reyner, 1991, American journal of human genetics.

Human Na(+)-myo-inositol cotransporter gene: alternate splicing generates diverse transcripts.

T. Glover, M. Togawa, F. Porcellati, 1998, The American journal of physiology.

Refined localization of human connexin32 gene locus, GJB1, to Xq13.1.

H. Willard, T. Glover, R. Loch-Caruso, 1992, Genomics.

The SNM1B/APOLLO DNA nuclease functions in resolution of replication stress and maintenance of common fragile site stability.

T. Glover, J. Sekiguchi, N. Patel, 2013, Human molecular genetics.

Localization of the genes encoding the melanocortin-2 (adrenocorticotropic hormone) and melanocortin-3 receptors to chromosomes 18p11.2 and 20q13.2-q13.3 by fluorescence in situ hybridization.

T. Glover, Y. Konda, T. Yamada, 1993, Genomics.

A novel VEGFR3 mutation causes Milroy disease

T. Glover, S. Rockson, M. G. Butler, 2007, American journal of medical genetics. Part A.

Clinical heterogeneity in lymphoedema-distichiasis withFOXC2 truncating mutations

Marilyn C. Jones, T. Glover, M. McDonald, 2001, Journal of medical genetics.

Mapping of the gene for interferon‐inducible dsRNA‐dependent protein kinase to chromosome region 2p21‐22: A site of rearrangements in myeloproliferative disorders

S. Hanash, N. Sonenberg, T. Glover, 1993, Genes, chromosomes & cancer.

Incontinentia pigmenti: occurrence in Arizona Indians and evidence against the half-chromatid mutation model.

F. Hecht, T. Glover, B. Kaiser‐Mccaw, 1982, Birth defects original article series.

Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).

T. Glover, B. Cox, W. Uhlmann, 1989, American journal of medical genetics.

Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting.

Stephen S. Gisselbrecht, James M. Harris, W. Goessling, 2011, American journal of human genetics.

Demethylation of repetitive DNA sequences in neuroblastoma

R. Kuick, S. Hanash, P. Ambros, 1996, Genes, chromosomes & cancer.

Identification and analysis of the human and murine putative chromatin structure regulator SUPT6H and Supt6h.

X. Chen, J. Korenberg, J. Cheng, 1996, Genomics.

A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints.

R. Shridhar, T. Glover, D. Smith, 1996, Genomics.

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

Laura Scott, Michael Boehnke, Peter Berglund, 2003, Nature.

A novel amplicon at 8p22-23 results in overexpression of cathepsin B in esophageal adenocarcinoma.

S Hanash, R Kuick, R. Kuick, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Locus-specific transcription silencing at the FHIT gene suppresses replication stress-induced copy number variant formation and associated replication delay

T. E. Wilson, T. Glover, M. Ljungman, 2021, Nucleic acids research.

Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice

P. Lockhart, T. Glover, A. Grimes, 1994, Nature Genetics.

Gene amplification of the Menkes (MNK; ATP7A) P-type ATPase gene of CHO cells is associated with copper resistance and enhanced copper efflux.

P. Lockhart, T. Glover, P. Shen, 1995, Human molecular genetics.

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

T. Glover, C. Keegan, B. Barshop, 2016, JIMD reports.

Isolation of a murine copper transporter gene, tissue specific expression and functional complementation of a yeast copper transport mutant.

D. Thiele, J. Lee, T. Glover, 2000, Gene.

Effects of harman and norharman on spontaneous and ultraviolet light-induced mutagenesis in cultured Chinese hamster cells.

J. Trosko, T. Glover, M. Castellazzi, 1978, Cancer research.

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

T. Glover, B. Yashar, C. Keegan, 2013, American journal of medical genetics. Part A.

Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition.

M. W. Glynn, T. Glover, 2005, Human molecular genetics.

Ultraviolet light induction of diphtheria toxin-resistant mutations in normal and DNA repair-deficient human and Chinese hamster fibroblasts.

J. Trosko, T. Glover, C. Chang, 1980, Basic life sciences.

DNA polymerase α inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes

T. Glover, C. Berger, Jane Coyle, 2004, Human Genetics.

Isolation of a partial candidate gene for Menkes disease by positional cloning

Thomas W. Glover, Paul Lockhart, P. Lockhart, 1993, Nature Genetics.

FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition.

T. Glover, Thomas W. Glover, 1981, American journal of human genetics.

Expression of fragile site on the human X chromosome in somatic cell hybrids between human fragile X cells and thymidylate synthase-negative mouse mutant cells.

T. Seno, T. Glover, D. Ayusawa, 1985, Japanese journal of cancer research : Gann.

Linkage and recombination between fragile X-linked mental retardation and the factor IX gene

S. Warren, T. Glover, P. Jagadeeswaran, 2004, Human Genetics.

The combined effects of FUdR addition and methionine depletion on the X-chromosome fragile site.

T. Glover, P. Howard‐Peebles, 1983, American journal of human genetics.

Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis

F. Collins, T. Glover, D. Marchuk, 1993, Nature Genetics.

Fragile sites in cancer: more than meets the eye

T. E. Wilson, T. Glover, M. Arlt, 2017, Nature Reviews Cancer.

Large transcription units unify copy number variants and common fragile sites arising under replication stress

T. E. Wilson, T. Glover, M. Ljungman, 2015, Genome research.

Activation of GATA binding protein 6 (GATA6) sustains oncogenic lineage-survival in esophageal adenocarcinoma

M. Meyerson, W. Lam, D. Beer, 2012, Proceedings of the National Academy of Sciences.

Multiple forms of genetic instability within a 2‐Mb chromosomal segment of 3q26.3–q27 are associated with development of esophageal adenocarcinoma

J. V. Moran, S. Gruber, D. Beer, 2006, Genes, chromosomes & cancer.

Genomic amplification of MET with boundaries within fragile site FRA7G and upregulation of MET pathways in esophageal adenocarcinoma

D. Beer, T. Giordano, Lin Lin, 2006, Oncogene.

Candidate Gene for this Amplicon as the Best Cyclin E Esophageal Adenocarcinomas Reveals Identification and Characterization of a 19 q 12 Amplicon in Updated

R. Kuick, S. Hanash, Zhou Zhu, 2000 .

Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: A putative Rho Rac guanine nucleotide exchange factor

R. Stevenson, C. Schwartz, M. Porteous, 1994, Cell.

The Hepatocyte Nuclear Factor 3 α Gene, HNF3α (FOXA1), on Chromosome Band 14q13 Is Amplified and Overexpressed in Esophageal and Lung Adenocarcinomas

David E. Misek, S. Hanash, D. Beer, 2002 .

The hepatocyte nuclear factor 3 alpha gene, HNF3alpha (FOXA1), on chromosome band 14q13 is amplified and overexpressed in esophageal and lung adenocarcinomas.

David E. Misek, S. Hanash, D. Beer, 2002, Cancer research.

Y;16 translocation breakpoint associated with a partial Turner phenotype identifies a foamy virus insertion

T. Glover, R. Erickson, S. Schmidt Drury, 1998, Cytogenetic and Genome Research.

FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites.

T. Glover, D. Smith, B. Hall, 1996, Human molecular genetics.

ATR Regulates Fragile Site Stability

T. Glover, P. Nghiem, A. Casper, 2002, Cell.

Stably transfected common fragile site sequences exhibit instability at ectopic sites

M. W. Glynn, T. Glover, M. Arlt, 2008, Genes, chromosomes & cancer.

Chromosome fragile sites.

T. Glover, Thomas W Glover, Sandra G Durkin, 2007, Annual review of genetics.

Common fragile sites.

T. Glover, 2006, Cancer letters.

BRCA1 Is Required for Common-Fragile-Site Stability via Its G2/M Checkpoint Function

M. Kastan, T. Glover, Bo Xu, 2004, Molecular and Cellular Biology.

FISH localization of the soluble thymidine kinase gene (TK1) to human 17q25, a region of chromosomal loss in sporadic breast tumors.

T. Glover, D. J. Law, A. L. Grant, 1996, Cytogenetics and cell genetics.

Mechanisms of common fragile site instability.

T. Glover, A. Casper, Sandra Durkin, 2005, Human molecular genetics.

Guidelines for the preparation and analysis of the fragile X chromosome in lymphocytes.

J. Fryns, U. Froster-Iskenius, T. Glover, 1991, American journal of medical genetics.

Fragile sites: overview, occurrence in acute nonlymphocytic leukemia and effects of caffeine on expression.

T. Glover, J. Coyle-Morris, R. Morgan, 1986, Cancer genetics and cytogenetics.

A yeast artificial chromosome contig encompassing the type 1 neurofibromatosis gene.

F. Collins, P. Taillon-Miller, B. Brownstein, 1992, Genomics.

Transcription elongation factor SII (TCEA) maps to human chromosome 3p22 --> p21.3.

S. Warren, T. Glover, D. Reines, 1996, Genomics.

A minimal critical region of the 8p22-23 amplicon in esophageal adenocarcinomas defined using sequence tagged site-amplification mapping and quantitative polymerase chain reaction includes the GATA-4 gene.

S. Hanash, D. Beer, M. Orringer, 2000, Cancer research.

Isolation of human and murine homologues of the Drosophila minibrain gene: human homologue maps to 21q22.2 in the Down syndrome "critical region".

T. Glover, L. Sternberg, S. H. Chung, 1996, Genomics.

A child with multiple congenital anomalies and karyotype 46,XY,del(14)(q31q32.3): further delineation of chromosome 14 interstitial deletion syndrome.

T. Glover, W. Uhlmann, J. Gorski, 1990, American journal of medical genetics.

Amplification and overexpression of the dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 2 (DYRK2) gene in esophageal and lung adenocarcinomas.

D. Beer, Lin Lin, M. Orringer, 2003, Cancer research.

Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines

F. Collins, D. Housman, D. Gutmann, 1993, Nature Genetics.

Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variants.

S. Warren, T. Glover, J. Mulle, 2009, American journal of human genetics.

Common fragile sites

T. Glover, A. Casper, M. Arlt, 2003, Cytogenetic and Genome Research.

De Novo CNV Formation in Mouse Embryonic Stem Cells Occurs in the Absence of Xrcc4-Dependent Nonhomologous End Joining

T. E. Wilson, T. Glover, M. Arlt, 2012, PLoS genetics.

Nine de novo duplications affecting both maternal and paternal chromosomes and an inherited 15q11.2 deletion, in a patient with developmental delay

T. Glover, J. Innis, M. Tayeh, 2015, Clinical case reports.

Mice hypomorphic for Atr have increased DNA damage and abnormal checkpoint response

T. Glover, T. Saunders, M. Arlt, 2009, Mammalian Genome.

Inhibition of topoisomerase I prevents chromosome breakage at common fragile sites.

T. Glover, M. Arlt, 2010, DNA repair.

Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome.

M. W. Glynn, T. Glover, R. Erickson, 2000, American journal of human genetics.

A methylated human 9-kb repetitive sequence on acrocentric chromosomes is homologous to a subtelomeric repeat in chimpanzees.

R. Kuick, S. Hanash, T. Glover, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Replication stress induces tumor-like microdeletions in FHIT/FRA3B

S. Warren, T. Glover, J. Mulle, 2008, Proceedings of the National Academy of Sciences.

Common fragile sites as targets for chromosome rearrangements.

T. Glover, Sandra Durkin, M. Arlt, 2006, DNA repair.

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

D. Beer, T. Glover, M. Arlt, 2002, Genes, chromosomes & cancer.

ATR Regulates Fragile Site Stability Common fragile sites are normally stable in cultured

T. Glover, P. Nghiem, A. Casper, 2002 .

Instability at chromosomal fragile sites.

T. Glover, 1998, Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer.

The characterization of the common fragile site FRA16D and its involvement in multiple myeloma translocations.

L. Roberts, T. Glover, K. Krummel, 2000, Genomics.

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

Erin McKean, B. Teh, R. Ferris, 2017, Head & neck.

Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation.

B. Emanuel, H. Kurahashi, T. Glover, 2014, Cancer genetics.

The canine copper toxicosis locus is not syntenic with ATP7B or ATX1 and maps to a region showing homology to human 2p21

T. Glover, G. Brewer, V. Yuzbasiyan-Gurkan, 1999, Mammalian Genome.

Aphidicolin-induced FRA3B breakpoints cluster in two distinct regions.

R. Shridhar, T. Glover, D. Smith, 1997, Genomics.

Cancer chromosome breakpoints and common fragile sites induced by aphidicolin.

F. Hecht, T. Glover, 1984, Cancer genetics and cytogenetics.

Distinct areas of allelic loss on chromosomal regions 10p and 10q in human prostate cancer.

T. Glover, J. Macoska, K. Wojno, 1996, Cancer research.

Frequent breakpoints in the 3p14.2 fragile site, FRA3B, in pancreatic tumors.

F. Sarkar, R. Shridhar, T. Glover, 1996, Cancer research.

Association of a mature B cell leukemia with a 4p+ chromosomal abnormality: derivation and characterization of a cell line.

R. Cody, J. Wasmuth, B. Mitchell, 1989, Leukemia.

The Fanconi anemia pathway is required for the DNA replication stress response and for the regulation of common fragile site stability.

A. D’Andrea, T. Glover, T. Taniguchi, 2005, Human molecular genetics.

FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.

Marlys H Witte, D. Jackson, T. Glover, 2003, Human molecular genetics.

Age of onset in hereditary lymphedema.

R. Ferrell, E. Feingold, T. Glover, 2003, The Journal of pediatrics.

Hydroxyurea induces de novo copy number variants in human cells

T. E. Wilson, T. Glover, Alev Cagla Ozdemir, 2011, Proceedings of the National Academy of Sciences.

Direct correlation between FRA3B expression and cigarette smoking

T. Glover, B. Glisson, C. Stein, 2002, Genes, chromosomes & cancer.

Microcell-mediated transfer of a single human chromosome complements xeroderma pigmentosum group A fibroblasts.

T. Glover, E. Friedberg, R. Schultz, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Molecular biology: Breaks in the brain

T. E. Wilson, T. Glover, 2016, Nature.

Breaking news on fragile sites in cancer.

T. E. Wilson, T. Glover, 2013, Cancer cell.

Replication stress and mechanisms of CNV formation.

T. E. Wilson, T. Glover, M. Arlt, 2012, Current opinion in genetics & development.

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

M. Vikkula, T. Glover, J. García-Pérez, 2012, American journal of medical genetics. Part A.

Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann–Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations

K. M. McSweeney, D. Nickerson, M. Bamshad, 2018, Human Genetics.

Harnessing genomics to identify environmental determinants of heritable disease.

M. Hurles, J. Lupski, P. Awadalla, 2013, Mutation research.

A "balanced" Y;16 translocation associated with Turner-like neonatal lymphedema suggests the location of a potential anti-Turner gene on the Y chromosome.

T. Glover, R. Erickson, J. Stone, 1995, Cytogenetics and cell genetics.

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

P. Hedera, T. Glover, J. Innis, 2012, American journal of medical genetics. Part A.

DNA demethylation induced by 5-azacytidine does not affect fragile X expression.

T. Glover, R. Gemmill, J. Coyle-Morris, 1986, American journal of human genetics.

A Gata2 intronic enhancer confers its pan-endothelia-specific regulation

J. D. Engel, T. Glover, Masayuki Yamamoto, 2007, Development.

A novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipital horn syndrome and not in Menkes disease.

T. Glover, J. Innis, S. Dagenais, 2001, American journal of human genetics.

Hypothesis: "Rogue cell"-type chromosomal damage in lymphocytes is associated with infection with the JC human polyoma virus and has implications for oncopenesis.

E. Major, B. Curfman, T. Glover, 1996, Proceedings of the National Academy of Sciences of the United States of America.

REV1 and polymerase ζ facilitate homologous recombination repair

T. Glover, C. Canman, Shilpy Sharma, 2011, Nucleic acids research.

fragile sites arising under replication stress Large transcription units unify copy number variants and common

T. E. Wilson, T. Glover, M. Ljungman, 2014 .

Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia.

T. Friedman, T. Glover, J. Innis, 1997, American journal of medical genetics.

Two-dimensional separation and cloning of chromosome 1 NotI-EcoRV-derived genomic fragments.

R. Kuick, S. Hanash, T. Glover, 1996, Genomics.

Polymerase chain reactions with alphoid‐repeat primers in combination with Alu or LINEs primers, generate chromosome‐specific DNA fragments

T. Glover, R. Erickson, M. Witt, 1991, Annals of human genetics.

Immunocytochemical Localization of the Menkes Copper Transport Protein (ATP7A) to the Trans-Golgi Network

T. Glover, J. Escara-Wilke, H. Dierick, 1997, Human molecular genetics.

Localization of the translocation breakpoint in a female with Menkes syndrome to Xq13.2-q13.3 proximal to PGK-1.

T. Glover, S. Wang, J. Higgins, 1991, American journal of human genetics.

Multicolor FISH mapping with Alu-PCR-amplified YAC clone DNA determines the order of markers in the BRCA1 region on chromosome 17q12-q21.

F. Collins, M. Boehnke, B. Weber, 1993, Genomics.

Severe anomalies associated with ring chromosome 7.

L. Biesecker, T. Glover, B. Cox, 1991, American journal of medical genetics.

Antibiotics containing trimethoprim and the fragile X chromosome.

F. Hecht, T. Glover, 1983, The New England journal of medicine.

Turning on and off recurrent balanced cortical activity

Michael Boehnke, Thomas W. Glover, Francis S. Collins, 2022 .

Mild phenotypic manifestation of a 7p15.3p21.2 deletion.

T. Glover, C. Wang, S. Maynard, 1993, Journal of medical genetics.

Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann–Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations

K. M. McSweeney, D. Nickerson, Jun Z. Li, 2018, Human Genetics.

Twin peaks: finding fragile sites with MiDAS-seq

T. E. Wilson, T. Glover, 2020, Cell Research.

Tissue distribution, genomic structure, and chromosome mapping of mouse and human eukaryotic initiation factor 4E-binding proteins 1 and 2.

H. Heng, S. Hanash, A. Gingras, 1996, Genomics.

Clarification of chromosomal abnormalities associated with sexual ambiguity by studies with Y-chromosomal DNA sequences.

T. Glover, R. Erickson, J. Stalvey, 1988, Cytogenetics and cell genetics.

Functional Interaction between the Fanconi Anemia D2 Protein and Proliferating Cell Nuclear Antigen (PCNA) via a Conserved Putative PCNA Interaction Motif*

T. Glover, N. Howlett, M. Rego, 2009, The Journal of Biological Chemistry.

Molecular and cytologic studies of Ehlers-Danlos syndrome type VIII.

L. Biesecker, T. Glover, R. Erickson, 1991, American journal of medical genetics.

Translocation breakpoint in Aarskog syndrome maps to Xp11.21 between ALAS2 and DXS323.

T. Glover, J. Gorski, J. Higgins, 1993, Human molecular genetics.

Fragile sites and X-linked retardation.

F. Hecht, B. Hecht, T. Glover, 1981, Hospital practice.

Fragile sites on chromosomes.

F. Hecht, T. Glover, B. Kaiser-Hecht, 1982, Pediatrics.

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

T. E. Wilson, T. Glover, M. Arlt, 2014, Environmental and molecular mutagenesis.

Fine mapping of X‐linked clasped thumb and mental retardation (MASA syndrome) in Xq28

T. Glover, E. Legius, J. Higgins, 1994, Clinical genetics.

Isolation and analysis of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: A putative rho/rac guanine nucleotide exchange factor

T. Glover, N. Pasteris, A. Cadle, 1994 .

Molecular structure of the Menkes disease gene (ATP7A).

T. Glover, J. Spencer, J. Mercer, 1995, Genomics.

Two highly polymorphic CA repeats in the Menkes gene (ATP7A)

T. Glover, J. Innis, H. Dierick, 1995, Human Genetics.

A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome

Leslie B Gordon, Francis S Collins, F. Collins, 2016, Journal of Medical Genetics.

SHORT COMMUNICATION Refined Localization of Human Connexin32 Gene Locus, GJBI, to Xql3.1

H. Willard, T. Glover, C. Begy, 1992 .

A somatic cell hybrid panel to facilitate identification of DNA sequences in the vicinity of the incontinentia pigmenti locus (IP1).

T. Glover, J. Gorski, C. Stein, 1989, Cytogenetics and cell genetics.

Sex pheromone production and perception in European corn borer moths is determined by both autosomal and sex-linked genes.

C. Löfstedt, T. Glover, B. Hansson, 1987, Proceedings of the National Academy of Sciences of the United States of America.