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Producer: 20190225
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903.
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904.
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Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea. [electronic resource] by
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In:
Breast (Edinburgh, Scotland) vol. 33
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Detecting splicing patterns in genes involved in hereditary breast and ovarian cancer. [electronic resource] by
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- Brault, Baptiste
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- Lemoine, Fréderic
- de la Grange, Pierre
- Guillaud-Bataille, Marine
- Caux-Moncoutier, Virginie
- Houdayer, Claude
- Bonnet, Françoise
- Blanc-Fournier, Cécile
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- Frebourg, Thierry
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In:
European journal of human genetics : EJHG vol. 25
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Peritoneal carcinomatosis after risk-reducing surgery in BRCA1/2 mutation carriers. [electronic resource] by
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Cancer vol. 124
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Pathology findings and clinical outcomes after risk reduction salpingo-oophorectomy in BRCA mutation carriers: a multicenter Spanish study. [electronic resource] by
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In:
Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico vol. 20
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Complete Remission Following Pembrolizumab in a Woman with Mismatch Repair-Deficient Endometrial Cancer and a Germline [electronic resource] by
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- Sullivan, Laura
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In:
The oncologist vol. 23
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A mouse model featuring tissue-specific deletion of p53 and Brca1 gives rise to mammary tumors with genomic and transcriptomic similarities to human basal-like breast cancer. [electronic resource] by
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- Silva, Grace O
- Pfefferle, Adam D
- Xiong, Jessie
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In:
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