𝔖 Bobbio Scriptorium
✦   LIBER   ✦

High resolution genomic analysis of 18q− using oligo-microarray comparative genomic hybridization (aCGH)

✍ Scribed by Patricia L. Heard; Erika M. Carter; AnaLisa C. Crandall; Courtney Sebold; Daniel E. Hale; Jannine D. Cody


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
352 KB
Volume
149A
Category
Article
ISSN
1552-4825

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Interstitial deletion of 18q: Comparativ
✍ Zenichiro Kato; Wataru Morimoto; Takeshi Kimura; Akihiro Matsushima; Naomi Kondo 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 168 KB 👁 1 views

## Abstract **BACKGROUND**: Interstitial deletion of chromosome 18q is rare, making it difficult to assign phenotypes to particular cytogenetic deletions. **CASE**: We present an 18‐year‐old female with an interstitial deletion of chromosome 18q21.2–q21.33. The clinical features included severe psy

Analysis of ovarian borderline tumors us
✍ Nancy G. Wolf; Fadi W. Abdul-Karim; Carol Farver; Evelin Schröck; Stanislas du M 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 340 KB 👁 2 views

It is unclear whether ovarian borderline tumors (tumors of low malignant potential) are independent entities or whether they are part of a continuum of tumor progression that culminates in ovarian carcinoma. Little is known about genetic abnormalities in borderline tumors because of the difficulty o

Genetic analysis of sorted Hodgkin and R
✍ Koichi Ohshima; Masako Ishiguro; Akiko Ohgami; Midori Sugihara; Seiji Haraoka; J 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 French ⚖ 272 KB 👁 1 views

Hodgkin and Reed-Sternberg (H and RS) cells are generally considered to be the neoplastic cells of Hodgkin's disease (HD); however, such cells are found only in a minority of HD lesions. Very few data have so far been published on the cyogenetic abnormalities in HD. An analysis of unknown genetic ab

Microarray-based comparative genomic hyb
✍ Angel Chao; Yun-Shien Lee; An-Shine Chao; Tzu-Hao Wang; Shuenn-Dyh Chang 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 241 KB 👁 1 views

## Background: Wolf-hirschhorn syndrome (whs), caused by the deletion of a segment in chromosome 4, is characterized by mental and developmental defects. clinical manifestations of whs include intrauterine growth restriction, failure to thrive in the neonatal period that is present simultaneously w