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Page 1
A comprehensive custom panel evaluation for routine hereditary cancer testing: improving the yield of germline mutation detection.
J Transl Med. 2020 Jun 10;18(1):232. doi: 10.1186/s12967-020-02391-z.
J Transl Med. 2020.
PMID: 32522261
Free PMC article.
A PALB2 truncating mutation: Implication in cancer prevention and therapy of Hereditary Breast and Ovarian Cancer.
Velázquez C, Esteban-Cardeñosa EM, Lastra E, Abella LE, de la Cruz V, Lobatón CD, Durán M, Infante M.
Velázquez C, et al. Among authors: de la cruz v.
Breast. 2019 Feb;43:91-96. doi: 10.1016/j.breast.2018.11.010. Epub 2018 Nov 29.
Breast. 2019.
PMID: 30521987
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Unraveling the molecular effect of a rare missense mutation in BRIP1 associated with inherited breast cancer.
Velázquez C, Esteban-Cardeñosa EM, Lastra E, Abella LE, de la Cruz V, Lobatón CD, Durán M, Infante M.
Velázquez C, et al. Among authors: de la cruz v.
Mol Carcinog. 2019 Jan;58(1):156-160. doi: 10.1002/mc.22910. Epub 2018 Sep 22.
Mol Carcinog. 2019.
PMID: 30230034
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Germline Genetic Findings Which May Impact Therapeutic Decisions in Families with a Presumed Predisposition for Hereditary Breast and Ovarian Cancer.
Velázquez C, K L, Esteban-Cardeñosa EM, Avila Cobos F, Lastra E, Abella LE, de la Cruz V, Lobatón CD, Claes KB, Durán M, Infante M.
Velázquez C, et al. Among authors: de la cruz v.
Cancers (Basel). 2020 Aug 3;12(8):2151. doi: 10.3390/cancers12082151.
Cancers (Basel). 2020.
PMID: 32756499
Free PMC article.
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Erlotinib or gefitinib as first-choice therapy for bronchorrhea in bronchioloalveolar carcinoma.
Sanz Rubiales A, de la Cruz V, Berezo JÁ, Torres MÁ.
Sanz Rubiales A, et al. Among authors: de la cruz v.
J Pain Symptom Manage. 2014 Jun;47(6):e7-9. doi: 10.1016/j.jpainsymman.2013.12.248. Epub 2014 Apr 18.
J Pain Symptom Manage. 2014.
PMID: 24747679
Free article.
No abstract available.
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