𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A multiplex PCR assay for routine evaluation of deletion of the short arm of chromosome 1 in neuroblastoma

✍ Scribed by G. Schleiermacher; M. Peter; J. Michon; J.-M. Zucker; G. Thomas; H. Magdelénat; O. Delattre


Book ID
116166194
Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
616 KB
Volume
31
Category
Article
ISSN
0959-8049

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Two distinct deleted regions on the shor
✍ Gudrun Schleiermacher; Martine Peter; Jean Michon; Jean-Pierre Hugot; Philippe V 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 526 KB

## Abstract The short arm of chromosome Ip is the most frequently altered chromosome segment in neuroblastoma. The alterations, mainly deletions, are thought to be indicative of the presence of a tumor suppressor gene. To further refine the chromosome localization of this gene, we have studied pair

Molecular evaluation of abnormalities of
✍ Jay D. Hunt; Dr. Allan Tereba 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 900 KB

## Abstract Cytogenetic analyses have documented the consistent deletion of part of the short arm of chromosome 1 in neuroblastoma cells suggesting the presence of a suppressor gene in this chromosomal region. To determine the smallest region of deletion overlap at the molecular level on independen

Interstitial deletion of the short arm o
✍ Mattia, Frank R. ;Wardinsky, Terrance D. ;Tuttle, Deborah J. ;Grix, Arthur ;Smit 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 323 KB 👁 2 views

## Abstract A male patient with a de novo proximal interstitial deletion of the short arm of chromosome 1 (46XY), del(1)(p13p22.3) is described with multiple anomalies and developmental delay. This patient's clinical manifestations are compared to previously reported patients with deletions of chro

A modified multiplex PCR assay for detec
✍ Yaping Wang; Waltraut Friedl; Marlies Sengteller; Matthias Jungck; Isabel Filges 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 379 KB

A method for detection of large genomic deletions in the MSH2 and MLH1 genes based on multiplex PCR and quantitative evaluation of PCR products is presented. All 35 exons of MSH2 and MLH1 were screened simultaneously in seven PCR reactions, each of them including primers for both genes. The method i