Works matching IS 13899600 AND DT 2017 AND VI 16 AND IP 3
Results: 20
Detection of false positive mutations in BRCA gene by next generation sequencing.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 311, doi. 10.1007/s10689-016-9955-8
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- Publication type:
- Article
Outcomes of retesting BRCA negative patients using multigene panels.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 319, doi. 10.1007/s10689-016-9956-7
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- Publication type:
- Article
The hereditary nature of small cell carcinoma of the ovary, hypercalcemic type: two new familial cases.
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- Familial Cancer, 2017, v. 16, n. 3, p. 395, doi. 10.1007/s10689-016-9957-6
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- Publication type:
- Article
Embryonal rhabdomyosarcoma in a patient with a heterozygous frameshift variant in the DICER1 gene and additional manifestations of the DICER1 syndrome.
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- Familial Cancer, 2017, v. 16, n. 3, p. 401, doi. 10.1007/s10689-016-9958-5
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- Publication type:
- Article
ATM mutations for surgeons.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 407, doi. 10.1007/s10689-016-9959-4
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- Publication type:
- Article
Identification of MSH2 inversion of exons 1-7 in clinical evaluation of families with suspected Lynch syndrome.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 357, doi. 10.1007/s10689-016-9960-y
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- Publication type:
- Article
Mutation screening of ACKR3 and COPS8 in kidney cancer cases from the CONFIRM study.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 411, doi. 10.1007/s10689-016-9961-x
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- Publication type:
- Article
Novel and reported pathogenic variants in exon 11 of BRCA2 gene in a cohort of Sri Lankan young breast cancer patients.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 329, doi. 10.1007/s10689-016-9962-9
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- Publication type:
- Article
A lesson from a reported pathogenic variant in Peutz-Jeghers syndrome: a case report.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 417, doi. 10.1007/s10689-016-9963-8
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- Publication type:
- Article
Psychosocial morbidity in TP53 mutation carriers: is whole-body cancer screening beneficial?
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- Familial Cancer, 2017, v. 16, n. 3, p. 423, doi. 10.1007/s10689-016-9964-7
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- Publication type:
- Article
Baseline results from the UK SIGNIFY study: a whole-body MRI screening study in TP53 mutation carriers and matched controls.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 433, doi. 10.1007/s10689-017-9965-1
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- Publication type:
- Article
Gastric tumours in FAP.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 363, doi. 10.1007/s10689-017-9966-0
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- Publication type:
- Article
Patients with negative multi-gene panel testing: a back to the future paradox?
- Published in:
- 2017
- By:
- Publication type:
- Letter
Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 441, doi. 10.1007/s10689-017-9968-y
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- Publication type:
- Article
The association between prognosis of breast cancer and first-degree family history of breast or ovarian cancer: a systematic review and meta-analysis.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 339, doi. 10.1007/s10689-017-9969-x
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- Publication type:
- Article
Supporting disclosure of genetic information to family members: professional practice and timelines in cancer genetics.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 447, doi. 10.1007/s10689-017-9970-4
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- Publication type:
- Article
Gastric cancer in FAP: a concerning rise in incidence.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 371, doi. 10.1007/s10689-017-9971-3
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- Publication type:
- Article
Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 377, doi. 10.1007/s10689-017-9972-2
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- Publication type:
- Article
Correlation between germline mutations in MMR genes and microsatellite instability in ovarian cancer specimens.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 351, doi. 10.1007/s10689-017-9973-1
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- Publication type:
- Article
Identification of a rare germline NBN gene mutation by whole exome sequencing in a lung-cancer survivor from a large family with various types of cancer.
- Published in:
- Familial Cancer, 2017, v. 16, n. 3, p. 389, doi. 10.1007/s10689-016-9954-9
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- Publication type:
- Article