| Q36883028 | A case-control study of paternal occupational exposures and the risk of childhood sporadic bilateral retinoblastoma |
| Q72228209 | Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification |
| Q33596814 | Application of PCR amplification of DNA from paraffin embedded tissue sections to linkage analysis in familial retinoblastoma |
| Q36891056 | Biological aspects of cytosine methylation in eukaryotic cells |
| Q40549905 | Biological basis of germline mutation: comparisons of spontaneous germline mutation rates among drosophila, mouse, and human |
| Q53514292 | Carcinogenesis. Is imprinting to blame? |
| Q73106258 | Clinical, cytogenetic, and molecular testing of Argentine patients with retinoblastoma |
| Q35889094 | Concordance between parental origin of chromosome 13q loss and chromosome 6p duplication in sporadic retinoblastoma |
| Q35194318 | Constitutional 1p36 deletion in a child with neuroblastoma. |
| Q24534231 | Constitutional mutations of the hSNF5/INI1 gene predispose to a variety of cancers |
| Q35249353 | Deletion of RB exons 24 and 25 causes low-penetrance retinoblastoma |
| Q58193482 | Diversity, parental germline origin, and phenotypic spectrum of de novoHRASmissense changes in Costello syndrome |
| Q68266640 | Embryonal tumours and genomic imprinting |
| Q30501651 | Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting |
| Q91474417 | Frequency of low-level and high-level mosaicism in sporadic retinoblastoma: genotype-phenotype relationships |
| Q37900028 | Gene amplification in human lung cancer. The myc family genes and other proto-oncogenes and growth factor genes |
| Q41461943 | Genetics of retinoblastoma: a study |
| Q72872602 | Genomic imprinting and gene activation in cancer |
| Q38367968 | Genomic imprinting in hereditary glomus tumours: evidence for new genetic theory |
| Q30501672 | Genomic imprinting: review and relevance to human diseases. |
| Q33958854 | Germline selection: population genetic aspects of the sexual/asexual life cycle |
| Q36293187 | How do retinoblastoma tumours form? |
| Q73728360 | Hypermethylation in the retinoblastoma gene is associated with unilateral, sporadic retinoblastoma |
| Q33676828 | Identification of RB1 germline mutations in Argentinian families with sporadic bilateral retinoblastoma |
| Q78483036 | Identification of novel mutations in the RB1 gene in Mexican patients with retinoblastoma |
| Q92897316 | Impact of yoga based lifestyle intervention on psychological stress and quality of life in the parents of children with retinoblastoma |
| Q45087026 | Kinesin family member 14: an independent prognostic marker and potential therapeutic target for ovarian cancer |
| Q38372956 | Management of retinoblastoma: opportunities and challenges. |
| Q35102210 | Maternal diet during pregnancy and unilateral retinoblastoma |
| Q35071315 | Medical radiation exposure and risk of retinoblastoma resulting from new germline RB1 mutation |
| Q36476823 | Molecular genetics in the pathology and diagnosis of retinoblastoma |
| Q30498610 | Molecular mechanisms of cancer |
| Q40410709 | Murine models of neoplasia: functional analysis of the tumour suppressor genes Rb-1 and p53. |
| Q37346472 | Mutation risk associated with paternal and maternal age in a cohort of retinoblastoma survivors |
| Q36794281 | Mutations in the RB1 gene and their effects on transcription |
| Q55480255 | No preferential loss of one parental allele of chromosome 17p13.3 in childhood medulloblastoma |
| Q33596715 | On the parental origin of de novo mutation in man. |
| Q30333986 | Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype |
| Q24672503 | Parent-of-origin effects in multiple endocrine neoplasia type 2B |
| Q50576090 | Parental age and childhood cancer risk: A Danish population-based registry study. |
| Q68615880 | Parental age in sporadic hereditary retinoblastoma |
| Q44196253 | Parental diet and risk of retinoblastoma resulting from new germline RB1 mutation |
| Q36569295 | Parental nutrient intake and risk of retinoblastoma resulting from new germline RB1 mutation |
| Q46021746 | Parental occupational exposures and the risk of childhood sporadic retinoblastoma: a report from the Children's Oncology Group. |
| Q43145454 | Parental origin of chromosome 22 alleles lost in meningioma |
| Q35198154 | Parental origin of de novo constitutional deletions of chromosomal band 11p13 |
| Q33910077 | Paternal germline origin and sex-ratio distortion in transmission of PTPN11 mutations in Noonan syndrome |
| Q52864973 | Paternal origin of new mutations in von Recklinghausen neurofibromatosis. |
| Q36338352 | Paternal selection favoring mutant alleles of the retinoblastoma susceptibility gene |
| Q36196113 | Perinatal characteristics and retinoblastoma |
| Q28249189 | Preferential amplification of the paternal allele of the N-myc gene in human neuroblastomas |
| Q72802833 | Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigrees |
| Q58347781 | Retinoblastoma |
| Q28658114 | Retinoblastoma and ambient exposure to air toxics in the perinatal period |
| Q79740077 | Retinoblastoma in India : microsatellite analysis and its application in genetic counseling |
| Q43156200 | Retinoblastoma linked with Seascale |
| Q41032011 | Retinoblastoma referral patterns in Saudi Arabia |
| Q35666011 | Similarity of spontaneous germinal and in vitro somatic cell mutation rates in humans: implications for carcinogenesis and for the role of exogenous factors in "spontaneous" germinal mutagenesis |
| Q36431511 | The RB1 gene mutation in a child with ectopic intracranial retinoblastoma |
| Q40873279 | The gene as theme in the paradigm of cancer |
| Q70117697 | The genetics of retinoblastoma |
| Q35889146 | The genetics of retinoblastoma, revisited |
| Q37671253 | The genetics of retinoblastoma. Relevance to the patient |
| Q40696542 | The scientific challenge of Langerhans cell histiocytosis |
| Q30499489 | Tumor-suppressor genes: cardinal factors in inherited predisposition to human cancers |
| Q36695776 | Very high incidence of germ cell tumorigenesis (seminomagenesis) in human papillomavirus type 16 transgenic mice |