The spectrum of RB1 germ-line mutations in hereditary retinoblastoma
about
RetinoblastomaCharacterization of mutations in patients with multiple endocrine neoplasia type 1.RB1 gene mutation up-date, a meta-analysis based on 932 reported mutations available in a searchable database.Drosophila as a Potential Model for Ocular TumorsCombined SSCP/duplex analysis by capillary electrophoresis for more efficient mutation detection.Genes and environment: effects on the development of second malignancies in retinoblastoma survivors.Mutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counsellingAnalysis of retinoblastoma age incidence data using a fully stochastic cancer model.Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosisA Rb1 promoter variant with reduced activity contributes to osteosarcoma susceptibility in irradiated mice.Mitotic recombination map of 13cen-13q14 derived from an investigation of loss of heterozygosity in retinoblastomas.Genotype-phenotype correlations in patients with retinoblastoma and interstitial 13q deletions.Identification of three novel RB1 mutations in Brazilian patients with retinoblastoma by "exon by exon" PCR mediated SSCP analysisParent-of-origin effects in SOX2 anophthalmia syndromeClinical stratification of glioblastoma based on alterations in retinoblastoma tumor suppressor protein (RB1) and association with the proneural subtypeMutational analysis of the RB1 gene in Moroccan patients with retinoblastoma.De novo mutational profile in RB1 clarified using a mutation rate modeling algorithmThe RB1 gene mutation in a child with ectopic intracranial retinoblastomaA parent-of-origin effect in two families with retinoblastoma is associated with a distinct splice mutation in the RB1 gene.Circulating tumor cells capture disease evolution in advanced prostate cancer.RB1 mutations and second primary malignancies after hereditary retinoblastoma.Minor lesion mutational spectrum of the entire NF1 gene does not explain its high mutability but points to a functional domain upstream of the GAP-related domain.Screening for large rearrangements of the RB1 gene in Iranian patients with retinoblastoma using multiplex ligation-dependent probe amplification.Genotyping of Polymorphic Microsatellite Markers Linked to RB1 Locus in Iranian Population.A Rapid and Sensitive Next-Generation Sequencing Method to Detect RB1 Mutations Improves Care for Retinoblastoma Patients and Their Families.Genetic screening in Iranian patients with retinoblastoma.
P2860
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P2860
The spectrum of RB1 germ-line mutations in hereditary retinoblastoma
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
The spectrum of RB1 germ-line mutations in hereditary retinoblastoma
@ast
The spectrum of RB1 germ-line mutations in hereditary retinoblastoma
@en
type
label
The spectrum of RB1 germ-line mutations in hereditary retinoblastoma
@ast
The spectrum of RB1 germ-line mutations in hereditary retinoblastoma
@en
prefLabel
The spectrum of RB1 germ-line mutations in hereditary retinoblastoma
@ast
The spectrum of RB1 germ-line mutations in hereditary retinoblastoma
@en
P2093
P2860
P1476
The spectrum of RB1 germ-line mutations in hereditary retinoblastoma
@en
P2093
Horsthemke B
Lohmann DR
Passarge E
P2860
P304
P407
P577
1996-05-01T00:00:00Z