| scholarly article | Q13442814 |
| P50 | author | Maria Isabel Achatz | Q42720491 |
| Silvia Regina Rogatto | Q85467617 | ||
| P2093 | author name string | A F Nóbrega | |
| L M Canto | |||
| R A R Villacis | |||
| T R Basso | |||
| P2860 | cites work | Germline copy number variation and cancer risk | Q37728292 |
| Molecular mechanisms of genomic imprinting and clinical implications for cancer | Q37831991 | ||
| The consequences of uniparental disomy and copy number neutral loss-of-heterozygosity during human development and cancer | Q37886251 | ||
| Aetiology, genetics and prevention of secondary neoplasms in adult cancer survivors | Q38093037 | ||
| Multiple primary cancers as a guide to heritability | Q38221583 | ||
| -7/7q- syndrome in myeloid-lineage hematopoietic malignancies: attempts to understand this complex disease entity | Q38226741 | ||
| Hereditary breast cancer syndromes and genetic testing | Q38266306 | ||
| Restoration of IGF2 imprinting by polycomb repressive complex 2 docking factor SUZ12 in colon cancer cells | Q38832417 | ||
| A population-based single nucleotide polymorphism array analysis of genomic aberrations in younger adult acute lymphoblastic leukemia patients | Q41366254 | ||
| Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers | Q41715495 | ||
| A Novel 23.1 Mb Interstitial Deletion Involving 7q22.3q32.1 in a Girl with Short Stature, Motor Delay, and Craniofacial Dysmorphism | Q41928305 | ||
| Testin is a tumor suppressor and prognostic marker in breast cancer | Q42831001 | ||
| Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia | Q24672211 | ||
| Clinicopathological relevance of BRAF mutations in human cancer | Q27278038 | ||
| Global cancer statistics, 2012 | Q27860501 | ||
| Frequent loss of imprinting of PEG1/MEST in invasive breast cancer | Q28146265 | ||
| Promoter switch: a novel mechanism causing biallelic PEG1/MEST expression in invasive breast cancer | Q28218774 | ||
| Differential expression of mimecan and thioredoxin domain-containing protein 5 in colorectal adenoma and cancer: a proteomic study | Q28250643 | ||
| Human chromosome fragility | Q28261002 | ||
| Inactivating CUX1 mutations promote tumorigenesis | Q28303563 | ||
| Cancer treatment and survivorship statistics, 2014 | Q29617702 | ||
| Pooled analysis of loss of heterozygosity in breast cancer: a genome scan provides comparative evidence for multiple tumor suppressors and identifies novel candidate regions | Q30476046 | ||
| Association between acquired uniparental disomy and homozygous mutations and HER2/ER/PR status in breast cancer | Q33770092 | ||
| Expanding the genetic basis of copy number variation in familial breast cancer. | Q33780936 | ||
| Integrative molecular profiling of triple negative breast cancers identifies amplicon drivers and potential therapeutic targets | Q33780945 | ||
| Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies | Q33788643 | ||
| DNA instability at chromosomal fragile sites in cancer | Q34152853 | ||
| Rare copy number variants observed in hereditary breast cancer cases disrupt genes in estrogen signaling and TP53 tumor suppression network | Q34318239 | ||
| NCG 5.0: updates of a manually curated repository of cancer genes and associated properties from cancer mutational screenings. | Q34499917 | ||
| copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer | Q34964524 | ||
| Incidence of multiple primary cancers and interval between first and second primary cancers | Q35051898 | ||
| New malignancies after squamous cell carcinoma and melanomas: a population-based study from Norway | Q35124575 | ||
| The Candidate Cancer Gene Database: a database of cancer driver genes from forward genetic screens in mice | Q35254569 | ||
| A clinical and genetic analysis of multiple primary cancer referrals to genetics services | Q35477924 | ||
| Patterns of somatic uniparental disomy identify novel tumor suppressor genes in colorectal cancer. | Q36139202 | ||
| Epigenetic instability of imprinted genes in human cancers | Q36370887 | ||
| Germline DNA copy number variation in familial and early-onset breast cancer | Q36393187 | ||
| Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma. | Q37180729 | ||
| Risk of second primary malignancies in women with breast cancer: Results from the European prospective investigation into cancer and nutrition (EPIC). | Q50962764 | ||
| LOH and copy neutral LOH (cnLOH) act as alternative mechanism in sporadic colorectal cancers with chromosomal and microsatellite instability. | Q53290401 | ||
| Splenic marginal zone lymphoma: characterization of 7q deletion and its value in diagnosis | Q61596133 | ||
| Increased frequency of 20q gain and copy-neutral loss of heterozygosity in mismatch repair proficient familial colorectal carcinomas | Q62978032 | ||
| Genomic profile of a Li-Fraumeni-like syndrome patient with a 45,X/46,XX karyotype, presenting neither mutations in TP53 nor clinical stigmata of Turner syndrome | Q63378058 | ||
| Refined mapping of the region of loss of heterozygosity on the long arm of chromosome 7 in human breast cancer defines the location of a second tumor suppressor gene at 7q22 in the region of the CUTL1 gene | Q77340270 | ||
| Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1→q31.1) | Q86516734 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 41677 | |
| P577 | publication date | 2017-01-31 | |
| P1433 | published in | Scientific Reports | Q2261792 |
| P1476 | title | Germline large genomic alterations on 7q in patients with multiple primary cancers | |
| P478 | volume | 7 |
Search more.