Works matching IS 17312302 AND DT 2021 AND VI 19 AND IP 1
Results: 50
Prevalence of germline TP53 mutation among early onset middle eastern breast cancer patients.
- Published in:
- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00206-w
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- Publication type:
- Article
Retroperitoneal leiomyosarcoma in a female patient with a germline splicing variant RAD51D c.904-2A > T: a case report.
- Published in:
- 2021
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- Publication type:
- Case Study
Correction to: Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis.
- Published in:
- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00203-z
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- Publication type:
- Article
Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis.
- Published in:
- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00203-z
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- Publication type:
- Article
Can harmful lifestyle, obesity and weight changes increase the risk of breast cancer in BRCA 1 and BRCA 2 mutation carriers? A Mini review.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00199-6
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- Article
Unusual course of disease and genetic profile in Li-Fraumeni syndrome-associated osteosarcoma – a case report.
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- 2021
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- Publication type:
- Case Study
"Left in limbo": Exploring how patients with colorectal cancer interpret and respond to a suspected Lynch syndrome diagnosis.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00201-1
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- Publication type:
- Article
Germline mutations among Polish patients with acute myeloid leukemia.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00200-2
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- Publication type:
- Article
Danish guidelines for management of non-APC-associated hereditary polyposis syndromes.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00197-8
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- Publication type:
- Article
Improving our model of cascade testing for hereditary cancer risk by leveraging patient peer support: a concept report.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00198-7
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- Article
Risk reduction strategies for BRCA1/2 hereditary ovarian cancer syndromes: a clinical practice guideline.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00196-9
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- Publication type:
- Article
Descriptive study on subjective experience of genetic testing with respect to relationship, family planning and psychosocial wellbeing among women with lynch syndrome.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00194-x
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- Publication type:
- Article
Correction to: Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Cytotoxic and targeted therapy for BRCA1/2-driven cancers.
- Published in:
- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00193-y
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- Publication type:
- Article
Population or family history based BRCA gene tests of breast cancer? A systematic review of economic evaluations.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00191-0
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- Publication type:
- Article
Myxofibrosarcoma harboring an MLH1 pathogenic germline variant associated with Muir-Torre syndrome: a case report.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00192-z
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- Publication type:
- Article
Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00190-1
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- Publication type:
- Article
Expanding the phenotype of E318K (c.952G > A) MITF germline mutation carriers: case series and review of the literature.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00189-8
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- Publication type:
- Article
Evaluation and comparison of hereditary Cancer guidelines in the population.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00188-9
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- Publication type:
- Article
Ultrasound guided needle biopsy of axilla to evaluate nodal metastasis after preoperative systemic therapy in cohort of 106 breast cancers enriched with BRCA1/2 pathogenic variant carriers.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00187-w
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- Publication type:
- Article
Deciding the operation type according to mismatch repair status among hereditary nonpolyposis colorectal cancer patients: should a tailored approach be applied, or does one size fit all?
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00186-x
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- Publication type:
- Article
A novel germline mutation in hMLH1 in three Korean women with endometrial cancer in a family of Lynch syndrome: case report and literature review.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00185-y
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- Publication type:
- Article
Correction to: Overview on population screening for carriers with germline mutations in mismatch repair (MMR) genes in China.
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- 2021
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- Publication type:
- Correction Notice
Overview on population screening for carriers with germline mutations in mismatch repair (MMR) genes in China.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00182-1
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- Publication type:
- Article
Overview on population screening for carriers with germline mutations in mismatch repair (MMR) genes in China.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00182-1
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- Publication type:
- Article
CD36 polymorphisms and the age of disease onset in patients with pathogenic variants within the mutation cluster region of APC.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00183-0
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- Publication type:
- Article
Impact of national guidelines on use of BRCA1/2 germline testing, risk management advice given to women with pathogenic BRCA1/2 variants and uptake of advice.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00180-3
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- Publication type:
- Article
Massive parallel sequencing in a family with rectal cancer.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00181-2
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- Publication type:
- Article
Should the BCRA1/2-mutations healthy carriers be valid candidates for hematopoietic stem cell donation?
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00179-w
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- Publication type:
- Article
CDKN2A germline alterations and the relevance of genotype-phenotype associations in cancer predisposition.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00178-x
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- Publication type:
- Article
Clinical implementation of an oncology‐specific family health history risk assessment tool.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00177-y
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- Publication type:
- Article
Assessment of genetic referrals and outcomes for women with triple negative breast cancer in regional cancer centres in Australia.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00176-z
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- Publication type:
- Article
Room for improvement: One third of Lynch syndrome patients presenting for genetic testing in a highly specialised centre in Stockholm already have cancer.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00171-4
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- Publication type:
- Article
Risk of hematological malignancies in the families of patients treated for nodular lymphocyte-predominant Hodgkin lymphoma.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00175-0
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- Publication type:
- Article
Clinical challenges in interpreting multiple pathogenic mutations in single patients.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00172-3
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- Publication type:
- Article
Neoadjuvant therapy of BRCA1-driven ovarian cancer by combination of cisplatin, mitomycin C and doxorubicin.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00173-2
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- Publication type:
- Article
BRCA1 and BRCA2 mutations in ovarian cancer patients from Belarus: update.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00169-y
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- Publication type:
- Article
Novel PHOX2B germline mutation in childhood medulloblastoma: a case report.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00170-5
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- Publication type:
- Article
A novel frequent BRCA1 recurrent variant c.5117G > A (p.Gly1206Glu) identified after 20 years of BRCA1/2 research in the Baltic region: cohort study and literature review.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00168-z
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- Publication type:
- Article
A rare large duplication of MLH1 identified in Lynch syndrome.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00167-0
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- Publication type:
- Article
Recontacting non-BRCA1/2 breast cancer patients for germline CHEK2 c.1100del pathogenic variant testing: uptake and patient experiences.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00166-1
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- Publication type:
- Article
Advanced adenomas may be a red flag for hereditary cancer syndromes.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-020-00164-9
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- Publication type:
- Article
Heterogeneous constitutional mismatch repair deficiency with MSH6 missense mutation clinically benefits from pembrolizumab and regorafenib combination therapy: a case report and literature review.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00165-2
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- Publication type:
- Article
Recurrent PALB2 mutations and the risk of cancers of bladder or kidney in Polish population.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-020-00161-y
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- Publication type:
- Article
Correction to: Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Familial pancreatic cancer with PALB2 and NBN pathogenic variants: a case report.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-020-00160-z
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- Publication type:
- Article
Metaplastic carcinoma of the breast and BRCA1 germline mutation: a case report and review.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-020-00162-x
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- Publication type:
- Article
Synchronous choroid plexus papilloma and Wilms tumor in a girl, disclosing a Li-Fraumeni syndrome.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-020-00158-7
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- Publication type:
- Article
Revisiting multiple erroneous genetic testing results and clinical misinterpretations in a patient with Li-Fraumeni syndrome: lessons for translational medicine.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-020-00157-8
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- Publication type:
- Article