Pages that link to "Q58048740"
Jump to navigation
Jump to search
The following pages link to Screening for germ line TP53 mutations in breast cancer patients (Q58048740):
Displaying 50 items.
- Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility (Q24679438) (← links)
- Cancer incidence in relatives of a population-based set of cases of early-onset breast cancer with a known BRCA1 and BRCA2 mutation status (Q24802534) (← links)
- The intronic G13964C variant in p53 is not a high-risk mutation in familial breast cancer in Australia (Q24806016) (← links)
- The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer (Q24806109) (← links)
- A Review of the Clinical Implications of Breast Cancer Biology (Q26744288) (← links)
- Association of the germline TP53 R337H mutation with breast cancer in southern Brazil (Q33388533) (← links)
- The TP53 gene rs1042522 C>G polymorphism and neuroblastoma risk in Chinese children (Q33563627) (← links)
- Prevalence of the TP53 p.R337H mutation in breast cancer patients in Brazil (Q33768942) (← links)
- The genetics of inherited breast cancer (Q33923794) (← links)
- Clinical management of hereditary breast cancer syndromes (Q34167563) (← links)
- Novel pattern of P53 mutation in breast cancers from Austrian women. (Q34201404) (← links)
- Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma (Q34207682) (← links)
- The role of p53 in human cancer (Q34283469) (← links)
- Late onset Li-Fraumeni Syndrome with bilateral breast cancer and other malignancies: case report and review of the literature (Q34294432) (← links)
- Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion (Q34301309) (← links)
- Tumor protein p53 (TP53) testing and Li-Fraumeni syndrome : current status of clinical applications and future directions (Q34324683) (← links)
- Li-Fraumeni syndrome – a molecular and clinical review (Q34432117) (← links)
- Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles (Q34586198) (← links)
- Characterization of familial breast cancer in Saudi Arabia (Q35042589) (← links)
- Intronic TP53 Germline Sequence Variants Modify the Risk in German Breast/Ovarian Cancer Families (Q35355110) (← links)
- Cancer risks from germline p53 mutations (Q35513831) (← links)
- Population-based estimate of the contribution of TP53 mutations to subgroups of early-onset breast cancer: Australian Breast Cancer Family Study (Q35587015) (← links)
- Germ-line p53 mutations in 15 families with Li-Fraumeni syndrome. (Q35643184) (← links)
- Tumors associated with p53 germline mutations: a synopsis of 91 families. (Q35765327) (← links)
- Prognostic significance of TP53 alterations in breast carcinoma (Q35976693) (← links)
- ABRAXAS (FAM175A) and Breast Cancer Susceptibility: No Evidence of Association in the Breast Cancer Family Registry (Q36043159) (← links)
- Cancer experience in the relatives of an unselected series of breast cancer patients. (Q36079492) (← links)
- The genetics of breast and ovarian cancer (Q36081587) (← links)
- Next-generation sequencing in familial breast cancer patients from Lebanon (Q36281775) (← links)
- Screening for TP53 mutations in patients and tumours from 109 Swedish breast cancer families (Q36420172) (← links)
- The R72P P53 mutation is associated with familial breast cancer in Jewish women (Q36616536) (← links)
- The genetics of breast cancer: risk factors for disease (Q36925187) (← links)
- Inherited and acquired alterations in development of breast cancer. (Q36925229) (← links)
- Breast cancer phenotype in women with TP53 germline mutations: a Li-Fraumeni syndrome consortium effort (Q37006537) (← links)
- Germ-line mutations of the p53 tumor suppressor gene in patients with high risk for cancer inactivate the p53 protein (Q37109203) (← links)
- Hereditary breast cancer: new genetic developments, new therapeutic avenues (Q37199029) (← links)
- Genomic Disparities in Breast Cancer Among Latinas. (Q37509093) (← links)
- Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21. (Q37684672) (← links)
- Breast Cancer Predisposition Syndromes (Q37785234) (← links)
- The complex genetic landscape of familial breast cancer (Q38095764) (← links)
- Next generation sequencing is informing phenotype: a TP53 example (Q38783154) (← links)
- Familial breast cancer and genes involved in breast carcinogenesis (Q40466587) (← links)
- Molecular Genetics and Cytogenetics of Sarcomas (Q40468269) (← links)
- Constitutional p53 mutations associated with brain tumors in young adults (Q46575531) (← links)
- Four separate regions on chromosome 17 show loss of heterozygosity in familial breast carcinomas (Q58862231) (← links)
- A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci (Q60925526) (← links)
- Functional Analysis of Promoter Variants in Genes Involved in Sex Steroid Action, DNA Repair and Cell Cycle Control (Q64087937) (← links)
- Oestrogen receptor (ESR) polymorphisms and breast cancer susceptibility (Q72878101) (← links)
- Bilateral Breast Cancer in a Patient with a Strong Family History of Cancer: Analysis of p53 Germ Line Mutations (Q73224007) (← links)
- Absence of germline and somatic p53 alterations in children with sporadic brain tumors (Q74418572) (← links)