SummaryIn most patients with isolated unilateral retinoblastoma, tumor development is initiated by somatic inactivation of both alleles of the RB1 gene. However, some of these patients can transmit retinoblastoma predisposition to their offspring. To determine the frequency and nature of constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma, we analyzed DNA from peripheral blood and from tumor tissue. The analysis of tumors from 54 (71%) of 76 informative patients showed loss of constitutional heterozygosity (LOH) at intragenic loci. Three of 13 uninformative patients had constitutional deletions. For 39 randomly selected tumors, SSCP, hetero-duplex analysis, sequencing, and Southern blot analysis were used t...
In retinoblastoma, two RB1 mutations are necessary for tumor development. Recurrent genomic rearrang...
Retinoblastoma (RB) is a rare childhood malignant disorder caused by the biallelic inactivation of R...
AbstractPurposeTo find correlation between the type of mutations observed and the severity of the di...
Retinoblastoma (RB) is a uncommon childhood malignant ailment induced by means of the biallelic inac...
Retinoblastoma, an embryonic neoplasm of retinal origin, is the most common primary intraocular mali...
Retinoblastoma (RB) is an inherited childhood ocular cancer caused by mutations in the tumor suppres...
<div><p>Retinoblastoma, an embryonic neoplasm of retinal origin, is the most common primary intraocu...
SummaryBackgroundRetinoblastoma is the childhood retinal cancer that defined tumour-suppressor genes...
Constitutional mutations in the RB1 gene predispose to retinoblastoma development. Hence genetic scr...
Retinoblastoma is a rare childhood cancer initiated by RB1 mutation or MYCN amplification, while add...
Retinoblastoma (RB) is the most common primary intraocular malignancy in children. Somatic inactivat...
PURPOSE: To study phenotype-genotype correlation in patients who have retinoma, which is a benign tu...
Twenty-one probands, twelve with bilateral and nine with unilateral retinoblastoma, were screened fo...
Background: Retinoblastoma (RB1; OMIM#180200) is the most common intraocular tumor in early childhoo...
Background Retinoblastoma (Rb) is a childhood cancer of the retina, commonly initiated by biallelic ...
In retinoblastoma, two RB1 mutations are necessary for tumor development. Recurrent genomic rearrang...
Retinoblastoma (RB) is a rare childhood malignant disorder caused by the biallelic inactivation of R...
AbstractPurposeTo find correlation between the type of mutations observed and the severity of the di...
Retinoblastoma (RB) is a uncommon childhood malignant ailment induced by means of the biallelic inac...
Retinoblastoma, an embryonic neoplasm of retinal origin, is the most common primary intraocular mali...
Retinoblastoma (RB) is an inherited childhood ocular cancer caused by mutations in the tumor suppres...
<div><p>Retinoblastoma, an embryonic neoplasm of retinal origin, is the most common primary intraocu...
SummaryBackgroundRetinoblastoma is the childhood retinal cancer that defined tumour-suppressor genes...
Constitutional mutations in the RB1 gene predispose to retinoblastoma development. Hence genetic scr...
Retinoblastoma is a rare childhood cancer initiated by RB1 mutation or MYCN amplification, while add...
Retinoblastoma (RB) is the most common primary intraocular malignancy in children. Somatic inactivat...
PURPOSE: To study phenotype-genotype correlation in patients who have retinoma, which is a benign tu...
Twenty-one probands, twelve with bilateral and nine with unilateral retinoblastoma, were screened fo...
Background: Retinoblastoma (RB1; OMIM#180200) is the most common intraocular tumor in early childhoo...
Background Retinoblastoma (Rb) is a childhood cancer of the retina, commonly initiated by biallelic ...
In retinoblastoma, two RB1 mutations are necessary for tumor development. Recurrent genomic rearrang...
Retinoblastoma (RB) is a rare childhood malignant disorder caused by the biallelic inactivation of R...
AbstractPurposeTo find correlation between the type of mutations observed and the severity of the di...