Sex chromosome loss in adults with haematological neoplasms von Cantú, Eduardo S., Moses, Michael D., Nemana, Lakshmi J., Pierre, Robert V.

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Discrepant Cytogenetic and Interphase Fluorescence In Situ Hybridization (I-FISH) Results from Bone Marrow Specimens of Patients with Hematologic Neoplasms von Cantú, Eduardo S, Dong, Henry, Forsyth, David R, Espinoza, Froilan P, Papenhausen, Peter R

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A Rare Case of Chronic Myelogenous Leukemia Presenting as T-Cell Lymphoblastic Crisis von Cantu, Eduardo S., El Behery, Radwa, Topalovski, Margarita, Padhi, Parikshit, Medavarapu, Ramadevi

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Male-to-female sex ratios of abnormalities detected by fluorescence in situ hybridization in a population of chronic lymphocytic leukemia patients von Cantú, Eduardo S, McGill, John R, Stephenson, Christine F, Hoffmann, Heidi M, Tang, Lihua, Yan, Jim, Glassman, Armand B

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The Frequency of Cytogenetic and FISH Abnormalities Is Higher in Female Than in Male Multiple Myeloma (MM) Patients von Cantu, Eduardo S, Szymanska, Jadwiga, Watson, Alan R, Trevizo, Sandy L, Rostami, Sassan

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Disproportionate Sex Chromosome Loss in Abnormal Karyotypes of Male and Female Patients with Diagnoses of Myeloid or Lymphoid Neoplasms von Cantu, Eduardo S., Nemana, Lakshmi, Pierre, Robert V., Moses, Mike

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Cytogenetic Profile of Plasma Cell Neoplasms with 1q21 (CKS1B) Gains: A Comparative Study Between Cytoplasmic Immunoglobulin (cIg) Fluorescence In Situ Hybridization (FISH) and Con... von Stephenson, Christine F., Berger, Carol S, Richmond, Lioudmila I, Edmiston, Jason P, Cantu, Eduardo S., Dong, Henry Y.

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All patients with the T(11;16)(q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders von ROWLEY, J. D, RESHMI, S, BEHM, F, DOGGETT, N. A, BORROW, J, ZELEZNIK-LE, N, SOBULO, O, MUSVEE, T, ANASTASI, J, RAIMONDI, S, SCHNEIDER, N. R, BARREDO, J. C, CANTU, E. S, SCHLEGELBERGER, B

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Molecular genetic approach to the characterization of the “Down syndrome region” of chromosome 21 von McCormick, Mary Kay, Schinzel, Albert, Petersen, Michael B., Stetten, Gail, Driscoll, Daniel J., Cantu, Eduardo S., Tranebjaerg, Lisbeth, Mikkelsen, Margareta, Watkins, Paul C., Antonarakis, Stylianos E.

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A Rare Case of Chronic Myelogenous Leukemia Presenting as T-Cell Lymphoblastic Crisis von Padhi, Parikshit, Topalovski, Margarita, El Behery, Radwa, Cantu, Eduardo S, Medavarapu, Ramadevi

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PIGMENTARY ABNORMALITIES AND CHROMOSOMAL AND GENETIC MOSAICISM AND CHIMERISM von Thomas, T, Cantu, Eduardo S, Frias, Jaime L

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Mosaic vs. nonmosaic trisomy 9: Report of a liveborn infant evaluated by fluorescence in situ hybridization and review of the literature von Cantú, Eduardo S., Eicher, Dorothea Jenkins, Shashidhar Pai, G., Donahue, Christopher J., Harley, Russell A.

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Paternal uniparental disomy of chromosome 15 in a child with angelman syndrome von Nicholls, Robert D., Pai, G. Shashidhar, Gottlieb, Wayne, Cantú, Eduardo S.

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Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21 von McCormick, Mary Kay, Schinzel, Albert, Petersen, Michael B, Stetten, Gail, Driscoll, Daniel J, Cantu, Eduardo S, Tranebjaerg, Lisbeth, Mikkelsen, Margareta, Watkins, Paul C, Antonarakis, Stylianos E

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Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation von Joseph, M, Cantú, E S, Pai, G S, Willi, S M, Papenhausen, P R, Weiss, L

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Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome von Tantravahi, Umadevi, Nicholls, Robert D., Stroh, Helene, Ringer, Steven, Neve, Rachael L., Kaplan, Lawrence, Wharton, Robert, Wurster-Hill, Doris, Graham Jr, John M., Cantú, Eduardo S., Frias, Jaime L., Kousseff, Boris G., Latt, Samuel A.

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The Human Palmitoyl-CoA Ligase (FACL2) Gene Maps to the Chromosome 4q34-q35 Region by Fluorescence in Situ Hybridization (FISH) and Somatic Cell Hybrid Panels von Cantú, Eduardo S., Sprinkle, Terry Joe, Ghosh, Bidyut, Singh, Inderjit

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Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotype von Williams, Charles A., Frias, Jaime L., McCormick, Mary Kay, Antonarakis, Stylianos E., Cantu, Eduardo S.

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Incidence of 15q deletions in the Angelman syndrome: A survey of twelve affected persons von Williams, Charles A., Gray, Brian A., Hendrickson, Jill E., Stone, John W., Cantú, Eduardo S.

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Recent experience in prenatal fra(X) detection von Jenkins, Edmund C., Brown, W. Ted, Krawczun, Michael S., Duncan, Charlotte J., Lele, Kusum P., Cantu, Eduardo S., Schonberg, Steven, Golbus, Mitchell S., Sekhon, Gurbax S., Stark, Sandra, Kunaporn, Suphat, Silverman, Wayne P.

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