Jacobsen syndrome is a rare congenital condition that’s caused by the deletion of several genes in chromosome 11. It’s sometimes called partial monosomy 11q. It occurs in about 1 in 100,000 ...

Jacobsen syndrome (JBS; MIM 147791), also called the 11q terminal deletion disorder (11q-), is a contiguous gene disorder caused by the deletion of the end of the long arm of chromosome 11. 1, 2 ...

A new four-story, 15-unit condominium building named 11Q stands at 11th and Q streets NW in the District, a stone’s throw from Logan Circle, the U Street corridor and 14th Street. The convenient ...

Jacobsen syndrome (JBS: OMIM 147791) is a contiguous gene syndrome resulting from the partial deletion of chromosome 11q. This syndrome was first described by Jacobsen in 1973. 1 The deletion size ...

Neuroblastoma is a childhood cancer with considerable morbidity and mortality. Tumor-derived biomarkers may improve risk stratification. We screened 915 samples of neuroblastoma for loss of heteroz ...

May 25, 2005 (Orlando) — Loss of heterozygosity on chromosome arm 11q is associated with a poor prognosis in neuroblastoma, according to findings presented here at the the American Society of ...

Article Title Systems biology network reveals the correlation between COX-2 expression and Ch 7q copy number alterations in Ch 11q-deleted pediatric neuroblastoma tumors ...