Pages that link to "Q34961418"
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The following pages link to Detection of mosaic RB1 mutations in families with retinoblastoma (Q34961418):
Displaying 50 items.
- Many mosaic mutations (Q28396430) (← links)
- A pathogenic mosaic TP53 mutation in two germ layers detected by next generation sequencing (Q33583996) (← links)
- Mutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counselling (Q33757922) (← links)
- Analysis of retinoblastoma age incidence data using a fully stochastic cancer model. (Q33841136) (← links)
- Enhanced sensitivity for detection of low-level germline mosaic RB1 mutations in sporadic retinoblastoma cases using deep semiconductor sequencing (Q33956073) (← links)
- Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation (Q34428954) (← links)
- Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma (Q35648428) (← links)
- Retinoblastoma genetics in India: From research to implementation (Q35663105) (← links)
- Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma. (Q35830949) (← links)
- Variation of second cancer risk by family history of retinoblastoma among long-term survivors (Q35925143) (← links)
- Alterations in the RB1 gene in Pakistani patients with retinoblastoma using direct sequencing analysis (Q36075348) (← links)
- Unifying cancer genetics (Q36142883) (← links)
- Next generation sequencing in sporadic retinoblastoma patients reveals somatic mosaicism (Q36184594) (← links)
- Risk of retinoblastoma is associated with a maternal polymorphism in dihydrofolatereductase (DHFR) and prenatal folic acid intake (Q36209893) (← links)
- Prediction and analysis of retinoblastoma related genes through gene ontology and KEGG. (Q37127244) (← links)
- Molecular analysis distinguishes metastatic disease from second cancers in patients with retinoblastoma (Q37146786) (← links)
- Screening of RB1 gene mutations in Chinese patients with retinoblastoma and preliminary exploration of genotype-phenotype correlations (Q37725058) (← links)
- The genomic landscape of retinoblastoma: a review (Q38179069) (← links)
- Secondary malignancies in pediatric cancer survivors: perspectives and review of the literature (Q38221521) (← links)
- Patient understanding of genetic information influences reproductive decision making in retinoblastoma. (Q38732120) (← links)
- Knowledge of genetics in familial retinoblastoma (Q38900429) (← links)
- Novel mutations in the RB1 gene from Chinese families with a history of retinoblastoma (Q38937782) (← links)
- Characterisation of retinoblastomas without RB1 mutations: genomic, gene expression, and clinical studies (Q39180520) (← links)
- Retinoblastoma and the genetic theory of cancer: an old paradigm trying to survive to the evidence (Q40171441) (← links)
- Screening for large rearrangements of the RB1 gene in Iranian patients with retinoblastoma using multiplex ligation-dependent probe amplification (Q41788572) (← links)
- Using RB1 mutations to assess minimal residual disease in metastatic retinoblastoma (Q42971686) (← links)
- Genotyping of Polymorphic Microsatellite Markers Linked to RB1 Locus in Iranian Population. (Q43061710) (← links)
- RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patients (Q44283852) (← links)
- Retinoblastoma pathway deregulatory mechanisms determine clinical outcome in high-grade serous ovarian carcinoma. (Q44568047) (← links)
- IVF and retinoblastoma revisited (Q44992278) (← links)
- Spectrum of RB1 mutations identified in 403 retinoblastoma patients. (Q46194694) (← links)
- A Rapid and Sensitive Next-Generation Sequencing Method to Detect RB1 Mutations Improves Care for Retinoblastoma Patients and Their Families. (Q46468588) (← links)
- Knowledge, experiences and attitudes concerning genetics among retinoblastoma survivors and parents (Q47706186) (← links)
- Incidental neuroblastoma with bilateral retinoblastoma: what are the chances? (Q47863034) (← links)
- Mutational analysis of the RB1 gene and the inheritance patterns of retinoblastoma in Jordan. (Q47959440) (← links)
- Robust identification of mosaic variants in congenital heart disease (Q50126566) (← links)
- Mosaicism and prenatal diagnosis options: insights from retinoblastoma (Q50357126) (← links)
- Genetic screening in Iranian patients with retinoblastoma (Q51075579) (← links)
- Mosaic partial deletion of the PTEN gene in a patient with Cowden syndrome (Q51155217) (← links)
- A novel deep intronic low penetrance RB1 variant in a retinoblastoma family. (Q52816352) (← links)
- Mutation spectrum of RB1 gene in Korean bilateral retinoblastoma patients using direct sequencing and gene dosage analysis. (Q53362178) (← links)
- Rapid detection of RB1 recurrent mutations in retinoblastoma by ARMS-PCR (Q57203751) (← links)
- Retinoblastoma (Q58347781) (← links)
- Parent-of-origin effect of hypomorphic pathogenic variants and somatic mosaicism impact on phenotypic expression of retinoblastoma (Q60367934) (← links)
- Spectrum of germline mutations and clinical manifestations in retinoblastoma patients from Thailand (Q60907558) (← links)
- Reproductive behavior of individuals with increased risk of having a child with retinoblastoma (Q85005985) (← links)
- Genetic screening in patients with Retinoblastoma in Israel (Q86895047) (← links)
- Low-level parental mosaicism in an apparent de novo case of Peutz-Jeghers syndrome (Q89285436) (← links)
- Frequency of low-level and high-level mosaicism in sporadic retinoblastoma: genotype-phenotype relationships (Q91474417) (← links)
- Next-Generation Technologies and Strategies for the Management of Retinoblastoma (Q91964988) (← links)