4 results match your criteria 1p36 1ptel

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Detection of deletions in 1q25, 1p36 and 1pTEL and chromosome 17 aneuploidy in oral epithelial dysplasia and oral squamous cell carcinoma by fluorescence in situ hybridization (FISH).

Oral Oncol 2021 Feb 17;116:105221. Epub 2021 Feb 17.

Department of Oral Pathology, University of Fortaleza / Universidade de Fortaleza, School of Dentistry, Fortaleza, Brazil.

Objective: To identify chromosome deletions in 1q25, 1p36 and 1pTEL, and chromosome 17 ploidy status in oral epithelial dysplasia (OED) and oral squamous cell carcinoma (OSCC).

Material And Methods: Samples from 57 OED and 63 OSCC were selected. FISH was performed using centromeric probes 17 and n LSIR 1p36/LSI 1q25 Dual Color Probe. Read More

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February 2021

Prenatal diagnosis of a fetus affected with Down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping.

Fetal Diagn Ther 2004 Jul-Aug;19(4):356-60

Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan.

Objective: A fetus having partial trisomy of the distal part of chromosome 21q due to a de novo translocation is reported here.

Method: A 29-year-old woman received amniocentesis at 18 weeks of gestation because of abnormal ultrasound findings including bilateral choroid plexus cysts, atrioventricular septal defects, rocker-bottom feet, and possible hydrocephalus.

Results: Cytogenetic analysis revealed 46,XY, add(1)(p36. Read More

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January 2005

Submicroscopic terminal deletion of 1p36.3 and Xp23 hidden in complex chromosome rearrangements: independent mechanism of telomere restitution on the two chromatids.

Am J Med Genet A 2003 Mar;117A(3):261-7

Quest Diagnostics, Inc., San Juan Capistrano, California, USA.

In this study, we report two cases each with a complex chromosome rearrangement concealing a submicroscopic terminal deletion. The first case had a mos 46,XX,der(1)t(1;9)(p36.3;p13). Read More

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Clinical categories of neuroblastoma are associated with different patterns of loss of heterozygosity on chromosome arm 1p.

J Mol Diagn 2000 Feb;2(1):37-46

Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.

Deletion of the short arm of chromosome 1 is frequently observed in neuroblastoma (NB). We performed loss of heterozygosity (LOH) analysis of 120 well characterized NB to better define specific regions of 1p loss and any association with clinical and biological prognostic features (DNA index, MYCN, age, and stage). All categories of disease were represented including 7 ganglioneuromas, 8 stage 4S, 33 local-regional (stages 1, 2, and 3), and 72 stage 4 NB according to the International Neuroblastoma Staging System. Read More

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February 2000
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