Search Results - "Cantú, Eduardo S."

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

“…Distorted sex ratios occur in hematologic disorders. For example, chronic lymphocytic leukemia (CLL) displays disproportionate sex ratios with a large male…”
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Sex chromosome loss in adults with haematological neoplasms by Cantú, Eduardo S., Moses, Michael D., Nemana, Lakshmi J., Pierre, Robert V.

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

“…Chronic Myelogenous Leukemia in blast crisis can manifest as either myeloid (more common) or lymphoid blast crisis. Most lymphoblastic crises are of B-cell…”
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The Frequency of Cytogenetic and FISH Abnormalities Is Higher in Female Than in Male Multiple Myeloma (MM) Patients by Cantu, Eduardo S, Szymanska, Jadwiga, Watson, Alan R, Trevizo, Sandy L, Rostami, Sassan

“…Sex determination in Homo sapiens is generally dependent on the inheritance of sex chromosome combination of XX (♀) or XY (♂). One could surmise that clinical…”
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Disproportionate Sex Chromosome Loss in Abnormal Karyotypes of Male and Female Patients with Diagnoses of Myeloid or Lymphoid Neoplasms by Cantu, Eduardo S., Nemana, Lakshmi, Pierre, Robert V., Moses, Mike

“…Sex chromosome loss (SCL) occurs in different types of human cells and is likely related to aging, but could also be related to other factors. We reviewed…”
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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 by Cantú, Eduardo S., Eicher, Dorothea Jenkins, Shashidhar Pai, G., Donahue, Christopher J., Harley, Russell A.

“…We report on a newborn infant with multiple congenital anomalies and apparent nonmosaic trisomy 9 in the blood (by conventional cytogenetic studies) who died…”
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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 Conventional FISH Involving 1283 Patients by Stephenson, Christine F., Berger, Carol S, Richmond, Lioudmila I, Edmiston, Jason P, Cantu, Eduardo S., Dong, Henry Y.

“…Abstract 3442▪▪This icon denotes a clinically relevant abstract Gains of 1q21 (CKS1B) in plasma cell neoplasms (PCNs) occur frequently and are generally…”
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Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome by Tantravahi, U, Nicholls, R D, Stroh, H, Ringer, S, Neve, R L, Kaplan, L, Wharton, R, Wurster-Hill, D, Graham, Jr, J M, Cantú, E S

“…Ten genomic DNA probes, subcloned from inserts derived from a phage library constructed from the DNA of flow-sorted chromosomes, have now been mapped to…”
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Paternal uniparental disomy of chromosome 15 in a child with Angelman syndrome by Nicholls, R D, Pai, G S, Gottlieb, W, Cantú, E S

“…Angelman and Prader-Willi syndromes are clinically distinct neurobehavioral disorders most commonly resulting from large deletions of chromosome 15q11-q13. The…”
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Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation by Joseph, M, Cantú, E S, Pai, G S, Willi, S M, Papenhausen, P R, Weiss, L

“…Colony stimulating factor-2 receptor alpha (CSF2RA) and interleukin-3 receptor alpha (IL3RA), two genes from the chromosome Xp and Yp pseudoautosomal region…”
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All patients with the T(11;16)(q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders by 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

“…The involvement of 11q23-balanced translocations in acute leukemia after treatment with drugs that inhibit the function of DNA topoisomerase II (topo II) is…”
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Mosaic trisomy 8: a cautionary note regarding missed antenatal diagnosis by Southgate, W M, Wagner, C L, Shields, S M, Cantú, E S, Pai, G S

“…Chromosomal analysis of fetal cells is a commonly used, safe, and highly accurate procedure. The rate of false-negative results is unknown. Recent experience…”
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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 by Cantú, Eduardo S., Sprinkle, Terry Joe, Ghosh, Bidyut, Singh, Inderjit

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Unusual cytogenetic mosaicism involving chromosome 14 abnormalities in a child with an MR/MCA syndrome and abnormal pigmentation by Cantú, E S, Thomas, I T, Frias, J L

“…An 8-year-old female child with mental retardation (MR), multiple congenital anomalies (MCA) and irregular pigmentation was shown to have karyotypic mosaicism…”
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Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons by Williams, C A, Gray, B A, Hendrickson, J E, Stone, J W, Cantú, E S

“…Prometaphase chromosome study of 12 persons with an established diagnosis of the Angelman syndrome demonstrated that 5 had a 15q12 deletion appearing similar…”
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Establishment of a cytogenetic service for chorionic villus samples: the split specimen approach by Cantú, E S, Ostrer, H, Gray, B A, Jackson, L G, Williams, C A

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Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21 by McCormick, M K, Schinzel, A, Petersen, M B, Stetten, G, Driscoll, D J, Cantu, E S, Tranebjaerg, L, Mikkelsen, M, Watkins, P C, Antonarakis, S E

“…The cytogenetically defined "Down syndrome region" of chromosome 21 has been characterized by DNA analysis in patients with partial trisomy 21 with or without…”
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A Rare Case of Chronic Myelogenous Leukemia Presenting as T-Cell Lymphoblastic Crisis by Padhi, Parikshit, Topalovski, Margarita, El Behery, Radwa, Cantu, Eduardo S, Medavarapu, Ramadevi

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Localization of chromosomal DNA sequences homologous to ribosomal gene type I insertion DNA in Drosophila melanogaster by Cantú, E S, Gay, H

“…Chromosomal sites which have DNA homology to the 1 kb (kilobase pair) BamHI restrictable fragment of the 5 kb type I insertion present in many ribosomal genes…”
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Fluorescence in situ hybridization (FISH) of a whole-arm translocation involving chromosomes 18 and 20 with alpha-satellite DNA probes: detection of a centromeric DNA break? by Cantú, E S, Khan, T A, Pai, G S

“…Fluorescence in situ hybridization (FISH) with alpha-satellite DNA probes was used to study whole-arm chromosome translocation products in a family in which…”
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