نتایج جستجو برای: deletion 6q

تعداد نتایج: 79891  

Journal: :Cancer research 1996
K A Cooney J C Wetzel C M Consolino K J Wojno

Allelic loss of 8p, 10q, 13q, 16q, and 18q has been frequently demonstrated in prostate cancer, implying the existence of putative tumor suppressor genes in these regions. However, there are likely a number of additional genetic events that define the progression from normal prostatic epithelium to prostate cancer that have yet to be identified. To characterize a novel region of deletion in spo...

Journal: :Blood 1996
X Y Guan D Horsman H E Zhang N Z Parsa P S Meltzer J M Trent

Deletion of the long arm of chromosome 6 (6q) is one of the most common chromosomal alterations in human B-cell lymphomas. Conventional cytogenetic banding analysis and loss-of-heterozygosity (LOH) studies have detected several common regions of deletion ranging across the entire long arm (6q), with no defined recurrent breakpoint yet identified. We describe here a strategy combining chromosome...

Journal: :Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2009
Stefan Pfister Marc Remke Axel Benner Frank Mendrzyk Grischa Toedt Jörg Felsberg Andrea Wittmann Frauke Devens Nicolas U Gerber Stefan Joos Andreas Kulozik Guido Reifenberger Stefan Rutkowski Otmar D Wiestler Bernhard Radlwimmer Wolfram Scheurlen Peter Lichter Andrey Korshunov

PURPOSE Medulloblastoma is the most common malignant brain tumor in children. Current treatment decisions are based on clinical variables. Novel tumor-derived biomarkers may improve the risk stratification of medulloblastoma patients. PATIENTS AND METHODS A model for the molecular risk stratification was proposed from an array-based comparative genomic hybridization (array-CGH) screen (n = 80...

Journal: :Kathmandu University medical journal 2012
L J Thapa B R Pokharel R Paudel P V S Rana

With the advances in neurogenetics association of epilepsy and intellectual disability with chromosomal abnormalities are being increasingly recognized. While onset of seizures with mental retardation at an early age indicate chromosomal abnormality, combination of characteristics facial dysmorphism and congenital abnormalities gives a clue of a particular syndrome. In addition MRI findings may...

Journal: :The Korean journal of laboratory medicine 2010
Kwang-Sook Woo Ji-Eun Kim Kyung-Eun Kim Myo-Jing Kim Jae-Ho Yoo Hyun-Sook Ahn Lisa G Shaffer Jin-Yeong Han

Deletions of chromosome 6q, particularly in the proximal region, are relatively rare. Here, we report on a de novo interstitial deletion of (6)(q13q16.2) in a girl with facial dysmorphism, congenital hip dislocation, porencephaly, and brain atrophy. Array comparative genomic hybridization analysis showed arr 6q13q16.2(73,378,824?99,824,130), demonstrating higher resolution than the conventional...

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