𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor

✍ Scribed by Jeanpierre, C.; Antignac, C.; Beroud, C.; Lavedan, C.; Henry, I.; Saunders, G.; Williams, B.; Glaser, T.; Junien, C.


Book ID
123536018
Publisher
Elsevier Science
Year
1990
Tongue
English
Weight
591 KB
Volume
7
Category
Article
ISSN
0888-7543

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


A constitutional bws-related t(11;16) ch
✍ Irene Newsham; Andrea Kindler-RΓΆhrborn; Douglas Daub; Webster Cavenee πŸ“‚ Article πŸ“… 1995 πŸ› John Wiley and Sons 🌐 English βš– 825 KB

## Abstract Beckwith‐Wiedemann syndrome (BWS) is a congenital overgrowth disorder with a varying spectrum of clinical manifestations including macroglossia, omphalocele, hemihypertrophy, and a predisposition to a subset of embryonal tumors, most frequently Wilms' tumor (WT). A variety of cytogeneti

Mutations/deletions of the WT1 gene, los
✍ Hisaya Nakadate; Kinji Yokomori; Naoki Watanabe; Takashi Tsuchiya; Takeshi Namik πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 French βš– 110 KB πŸ‘ 2 views

## Incidence rates of Wilms' tumor (WT) markedly differ in East Asian and Caucasian children. In the present study, we examined WT1 deletions/mutations and loss of heterozygosity (LOH) on 11p and 11q in a large number of WTs and compared our findings with those from 4 series of Caucasian WTs. Inci

Testicular germ cell tumors of adults sh
✍ Dr. Leendert H. J. Looijenga; Ad J. M. Gillis; J. Wolter Oosterhuis; Mary Abraha πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 669 KB

We have studied the involvement of chromosomal bands I I p I 3 and I I p 15.5 in I 5 testicular seminomas (SE) and I8 testicular nonseminomatous germ cell tumors (NS). NO allelic imbalances were found in 40% of the SE and 44% of the NS. LOSS of heterozygosity (LOH) at I I p 15.5 was seen in 2 I % of