E S Cantu
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Explore the profile of E S Cantu including associated specialties, affiliations and a list of published articles.
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Articles
25
Citations
309
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Recent Articles
1.
Southgate W, Wagner C, Shields S, Cantu E, Pai G
J Perinatol
. 1998 Apr;
18(1):78-80.
PMID: 9527951
Chromosomal analysis of fetal cells is a commonly used, safe, and highly accurate procedure. The rate of false-negative results is unknown. Recent experience at four centers suggests that there may...
2.
Rowley J, Reshmi S, Sobulo O, Musvee T, Anastasi J, Raimondi S, et al.
Blood
. 1997 Jul;
90(2):535-41.
PMID: 9226152
The involvement of 11q23-balanced translocations in acute leukemia after treatment with drugs that inhibit the function of DNA topoisomerase II (topo II) is being recognized with increasing frequency. We and...
3.
Laver J, Yusuf U, Cantu E, Barredo J, HOLT L, Abboud M
Leukemia
. 1997 Mar;
11(3):448-50.
PMID: 9067588
Secondary acute myelocytic leukemia (AML) and myelodysplastic syndromes (MDS) are known to develop in patients previously treated with different chemotherapeutic regimens. Nonrandom chromosomal abnormalities have been demonstrated in these therapy-related...
4.
Joseph M, Cantu E, Pai G, Willi S, Papenhausen P, WEISS L
J Med Genet
. 1996 Nov;
33(11):906-11.
PMID: 8950669
Colony stimulating factor-2 receptor alpha (CSF2RA) and interleukin-3 receptor alpha (IL3RA), two genes from the chromosome Xp and Yp pseudoautosomal region (PAR), have been suggested as candidate genes for short...
5.
Cantu E, Eicher D, Pai G, Donahue C, Harley R
Am J Med Genet
. 1996 Apr;
62(4):330-5.
PMID: 8723059
We report on a newborn infant with multiple congenital anomalies and apparent nonmosaic trisomy 9 in the blood (by conventional cytogenetic studies) who died shortly after birth. Clinical observations at...
6.
Cantu E, Sprinkle T, Ghosh B, Singh I
Genomics
. 1995 Aug;
28(3):600-2.
PMID: 7490105
No abstract available.
7.
Cantu E, Jacobs D, Pai G
Ann Clin Lab Sci
. 1995 Jan;
25(1):60-5.
PMID: 7762970
Small marker chromosomes (SMC) associated with severe Turner syndrome (TS) variants often represent reduced X chromosomes lacking the X inactivation center (XIC), perturbed dosage compensation, and unbalanced gene expression. A...
8.
Cantu E, Khan T, Pai G
Am J Med Genet
. 1992 Oct;
44(3):340-4.
PMID: 1488982
Fluorescence in situ hybridization (FISH) with alpha-satellite DNA probes was used to study whole-arm chromosome translocation products in a family in which the propositus was shown to have a monosomy...
9.
Nicholls R, Pai G, Gottlieb W, Cantu E
Ann Neurol
. 1992 Oct;
32(4):512-8.
PMID: 1360787
Angelman and Prader-Willi syndromes are clinically distinct neurobehavioral disorders most commonly resulting from large deletions of chromosome 15q11-q13. The deletions arise differentially during maternal or paternal gametogenesis, respectively. A subgroup...
10.
Williams C, Zori R, Stone J, Gray B, Cantu E, Ostrer H
Am J Med Genet
. 1990 Mar;
35(3):350-3.
PMID: 2309781
Six persons with the classical Angelman syndrome (AS) phenotype and de novo deletions of chromosome 15q11-q13 were studied to determine the parental origin of the chromosome deletion. Four of the...