Works matching IS 13899600 AND DT 2022 AND VI 21 AND IP 1
Results: 14
Age of diagnosis in familial Barrett's associated neoplasia.
- Published in:
- Familial Cancer, 2022, v. 21, n. 1, p. 115, doi. 10.1007/s10689-021-00239-z
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- Publication type:
- Article
Knowledge and psychosocial impact of genetic counseling and multigene panel testing among individuals with ovarian cancer.
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- Familial Cancer, 2022, v. 21, n. 1, p. 35, doi. 10.1007/s10689-021-00240-6
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- Article
Use of sanger and next-generation sequencing to screen for mosaic and intronic APC variants in unexplained colorectal polyposis patients.
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- Familial Cancer, 2022, v. 21, n. 1, p. 79, doi. 10.1007/s10689-021-00236-2
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- Article
Managing gastric cancer risk in lynch syndrome: controversies and recommendations.
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- Familial Cancer, 2022, v. 21, n. 1, p. 75, doi. 10.1007/s10689-021-00235-3
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- Publication type:
- Article
The needs of Southeast Asian BRCA mutation carriers considering risk-reducing salpingo-oophorectomy: a qualitative study.
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- Familial Cancer, 2022, v. 21, n. 1, p. 21, doi. 10.1007/s10689-021-00232-6
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- Publication type:
- Article
Approach to screening for Familial Adenomatous Polyposis (FAP) in a cohort of 226 patients with Desmoid-type Fibromatosis (DF): experience of a specialist center in the UK.
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- Familial Cancer, 2022, v. 21, n. 1, p. 69, doi. 10.1007/s10689-021-00230-8
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- Publication type:
- Article
Genetic predisposition to prostate cancer: an update.
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- Familial Cancer, 2022, v. 21, n. 1, p. 101, doi. 10.1007/s10689-021-00227-3
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- Article
Comparison of universal screening in major lynch-associated tumors: a systematic review of literature.
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- Familial Cancer, 2022, v. 21, n. 1, p. 57, doi. 10.1007/s10689-020-00226-w
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- Publication type:
- Article
Progress Report: New insights into the prevention of CRC by colonoscopic surveillance in Lynch syndrome.
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- Familial Cancer, 2022, v. 21, n. 1, p. 49, doi. 10.1007/s10689-020-00225-x
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- Publication type:
- Article
Correction to: Infantile fibrosarcoma with TPN3-NTRK3 fusion in a boy with Bloom Syndrome.
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- Familial Cancer, 2022, v. 21, n. 1, p. 91, doi. 10.1007/s10689-020-00223-z
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- Publication type:
- Article
Genetic evaluation of patients and families with concern for hereditary endocrine tumor syndromes.
- Published in:
- Familial Cancer, 2022, v. 21, n. 1, p. 93, doi. 10.1007/s10689-020-00222-0
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- Publication type:
- Article
Infantile fibrosarcoma with TPM3-NTRK1 fusion in a boy with Bloom syndrome.
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- 2022
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- Publication type:
- Case Study
Atypical choroidal nevus in a subject with a germline PALB2 pathogenic variant.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
Interpretation of BRCA2 Splicing Variants: A Case Series of Challenging Variant Interpretations and the Importance of Functional RNA Analysis.
- Published in:
- Familial Cancer, 2022, v. 21, n. 1, p. 7, doi. 10.1007/s10689-020-00224-y
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- Publication type:
- Article