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
## 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
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
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
## 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