C. Harris

发表

Use of fluorescent in situ hybridization to detect trisomy 13 in archival tissues for cytogenetic diagnosis.

R. Drut, L. Meisner, C. Harris, 1992, Pediatric pathology.

Short Communication Genome-Wide Appraisal of Thyroid Cancer Progression

J. Shah, Bhuvanesh Singh, P. Rao, 2002 .

FISH detection of HER-2/neu oncogene amplification in early onset breast cancer

K. Gilchrist, L. Meisner, C. Harris, 2005, Breast Cancer Research and Treatment.

Use of nonbreakpoint DNA probes to detect the t(X;18) in interphase cells from synovial sarcoma: implications for detection of diagnostic tumor translocations.

L. Meisner, D. Steiner, C. Harris, 1998, The American journal of pathology.

Identical Cytogenetic Clones and Clonal Evolution in Pediatric Monozygotic Twins With Acute Myeloid Leukemia: Presymptomatic Disease Detection by Interphase Fluorescence In Situ Hybridization and Review of the Literature

L. Meisner, T. Loew, C. Harris, 1998, Journal of pediatric hematology/oncology.

Granulocytic Sarcoma Presenting as Pneumonia in a Child With t(8;21) Acute Myelogenous Leukemia: Diagnosis by Fluorescent In Situ Hybridization

P. Rao, C. Lau, Dean Anthony Lee, 2004, Journal of pediatric hematology/oncology.

Use of FISH to detect chromosomal translocations and deletions. Analysis of chromosome rearrangement in synovial sarcoma cells from paraffin-embedded specimens.

S. Shim, L. Meisner, Wonbae Lee, 1993, The American journal of pathology.

Use of fluorescent in situ hybridization to detect aneuploidy in cervical dysplasia

L. Meisner, D. Kurtycz, C. Harris, 1996, Diagnostic cytopathology.

Cytogenetic abnormalities in renal oncocytic neoplasms

V. Speights, K. Scott Coffield, S. Dobin, 1992, Genes, chromosomes & cancer.

Genetic analysis identifies putative tumor suppressor sites at 2q35–q36.1 and 2q36.3–q37.1 involved in cervical cancer progression

M. Mansukhani, P. Rao, M. Terry, 2003, Oncogene.

Quantifying chromosome changes and lineage involvement in myelodysplastic syndrome (MDS) using fluorescent in situ hybridization (FISH).

L. Meisner, K. Han, S. Shim, 1994, Leukemia.

HER-2/neu gene amplification characterized by fluorescence in situ hybridization: poor prognosis in node-negative breast carcinomas.

D. Slamon, M. Press, L. Meisner, 1997, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Deletion of 1p32-p36 Is the Most Frequent Genetic Change and Poor Prognostic Marker in Adenoid Cystic Carcinoma of the Salivary Glands

R. Weber, P. Rao, D. Bell, 2008, Clinical Cancer Research.

Genome-wide appraisal of thyroid cancer progression.

J. Shah, Bhuvanesh Singh, P. Rao, 2002, The American journal of pathology.

Molecular determinants of tumor differentiation in papillary serous ovarian carcinoma

C. Sotiriou, A. Jazaeri, E. Liu, 2003, Molecular carcinogenesis.

Chromosomal amplifications, 3q gain and deletions of 2q33-q37 are the frequent genetic changes in cervical carcinoma

P. Rao, M. Terry, Fang F. Zhang, 2004, BMC Cancer.

Use of fluorescence in situ hybridization for retrospective detection of aneuploidy in multiple myeloma

L. Meisner, Wonbae Lee, C. Harris, 1993, Genes, chromosomes & cancer.

Comparison of chromosome aberrations in leiomyoma and leiomyosarcoma using FISH on archival tissues.

L. Meisner, C. Kang, K. Han, 1994, Cancer genetics and cytogenetics.

Genome-wide array comparative genomic hybridization analysis reveals distinct amplifications in osteosarcoma

Shishir Shah, Tsz-Kwong Man, Marc Ladanyi, 2004, BMC Cancer.

Frequent amplification and rearrangement of chromosomal bands 6p12‐p21 and 17p11.2 in osteosarcoma

A. Huvos, P. Rao, C. Lau, 2004, Genes, chromosomes & cancer.

Multicolor spectral karyotyping of serous ovarian adenocarcinoma

S. Mok, P. Rao, C. Lau, 2002, Genes, chromosomes & cancer.

A juvenile polyposis tumor suppressor locus at 10q22 is deleted from nonepithelial cells in the lamina propria.

L. Meisner, R F Jacoby, S Schlack, 1997, Gastroenterology.

Detection of aneuploidy and possible deletion in paraffin-embedded rhabdomyosarcoma cells with FISH.

L. Meisner, K. Han, W. Lee, 1993, Cancer genetics and cytogenetics.

Comprehensive molecular cytogenetic characterization of cervical cancer cell lines

Bhuvanesh Singh, P. Rao, G. Narayan, 2003, Genes, chromosomes & cancer.

Comparison of fluorescence in situ hybridization and primed in situ labeling methods for detection of single-copy genes in the fungus Ustilago maydis

S. Leong, Shuxian Li, C. Harris, 1993 .

Heteropagus conjoined twins due to fusion of two embryos: report and review.

L. Meisner, R. Logroño, C. Harris, 1997, American journal of medical genetics.

Use of fine needle aspiration for fibroblast culture.

R. Logroño, D. Kurtycz, S. Asplund, 1998, Pediatric pathology & laboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association.

Potential use of buccal smears for rapid diagnosis of autosomal trisomy or chromosomal sex in newborn infants using DNA probes.

L. Meisner, K. Clark, C. Harris, 1994, American journal of medical genetics.