Works matching IS 17312302 AND DT 2021 AND VI 19 AND IP 1

Results: 50
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    Germline mutations among Polish patients with acute myeloid leukemia.

    Published in:
    Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00200-2
    By:
    • Bąk, Aneta;
    • Skonieczka, Katarzyna;
    • Jaśkowiec, Anna;
    • Junkiert-Czarnecka, Anna;
    • Heise, Marta;
    • Pilarska-Deltow, Maria;
    • Potoczek, Stanisław;
    • Czyżewska, Maria;
    • Haus, Olga
    Publication type:
    Article
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    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.

    Published in:
    Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00180-3
    By:
    • Meiser, Bettina;
    • Kaur, Rajneesh;
    • Morrow, April;
    • Peate, Michelle;
    • Wong, W. K. Tim;
    • McPike, Emily;
    • Cops, Elisa;
    • Nichols, Cassandra;
    • Austin, Rachel;
    • Fine, Miriam;
    • Thrupp, Letitia;
    • Ward, Robyn;
    • Macrae, Finlay;
    • Hiller, Janet E.;
    • Trainer, Alison H.;
    • Mitchell, Gillian;
    • for the ICCon Audit Study Collaborative Group;
    • Susman, R.;
    • Pachter, N.;
    • Goodwin, A.
    Publication type:
    Article
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    Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants.

    Published in:
    Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00190-1
    By:
    • Murali, Krithika;
    • Dwarte, Tanya M.;
    • Nikfarjam, Mehrdad;
    • Tucker, Katherine M.;
    • Vaughan, Rhys B.;
    • Efthymiou, Marios;
    • Collins, Allison;
    • Spigelman, Allan D.;
    • Salmon, Lucinda;
    • Johns, Amber L.;
    • Williams, David B.;
    • Delatycki, Martin B.;
    • John, Thomas;
    • Stoita, Alina
    Publication type:
    Article
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    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.

    Published in:
    Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00187-w
    By:
    • Līcīte, Baiba;
    • Irmejs, Arvīds;
    • Maksimenko, Jeļena;
    • Loža, Pēteris;
    • Trofimovičs, Genādijs;
    • Miklaševičs, Edvīns;
    • Nazarovs, Jurijs;
    • Romanovska, Māra;
    • Deičmane, Justīne;
    • Irmejs, Reinis;
    • Purkalne, Gunta;
    • Gardovskis, Jānis
    Publication type:
    Article
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    Massive parallel sequencing in a family with rectal cancer.

    Published in:
    Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00181-2
    By:
    • Wallander, Karin;
    • Thutkawkorapin, Jessada;
    • Sahlin, Ellika;
    • Lindblom, Annika;
    • Lagerstedt-Robinson, Kristina
    Publication type:
    Article
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    Assessment of genetic referrals and outcomes for women with triple negative breast cancer in regional cancer centres in Australia.

    Published in:
    Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00176-z
    By:
    • Hallenstein, Lucie G.;
    • Sorensen, Carol;
    • Hodgson, Lorraine;
    • Wen, Shelly;
    • Westhuyzen, Justin;
    • Hansen, Carmen;
    • Last, Andrew T. J.;
    • Amalaseelan, Julan V.;
    • Salindera, Shehnarz;
    • Ross, William;
    • Spigelman, Allan D.;
    • Shakespeare, Thomas P.;
    • Aherne, Noel J.
    Publication type:
    Article
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    Novel PHOX2B germline mutation in childhood medulloblastoma: a case report.

    Published in:
    Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00170-5
    By:
    • Ke, Caiping;
    • Shi, Xiaoshun;
    • Chen, Allen Menglin;
    • Li, Chaoming;
    • Jiang, Bifeng;
    • Huang, Kailing;
    • Zheng, Zhouxia;
    • Liu, Yanhui;
    • Chen, Zhuona;
    • Luo, Yingjun;
    • Lin, Huaming;
    • Zhang, Jiexia
    Publication type:
    Article
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    A rare large duplication of MLH1 identified in Lynch syndrome.

    Published in:
    Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00167-0
    By:
    • Kumar, Abhishek;
    • Paramasivam, Nagarajan;
    • Bandapalli, Obul Reddy;
    • Schlesner, Matthias;
    • Chen, Tianhui;
    • Sijmons, Rolf;
    • Dymerska, Dagmara;
    • Golebiewska, Katarzyna;
    • Kuswik, Magdalena;
    • Lubinski, Jan;
    • Hemminki, Kari;
    • Försti, Asta
    Publication type:
    Article
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    Metaplastic carcinoma of the breast and BRCA1 germline mutation: a case report and review.

    Published in:
    Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-020-00162-x
    By:
    • Yamashita, Michiko;
    • Kamei, Yoshiaki;
    • Murakami, Akari;
    • Ozaki, Erina;
    • Okujima, Kumiko;
    • Takemoto, Kana;
    • Takaoka, Megumi;
    • Tsukamoto, Daiki;
    • Kusakabe, Erina;
    • Shidahara, Tomoyuki;
    • Noda, Haruna;
    • Aoki, Reina;
    • Taguchi, Kana;
    • Nishiyama, Kanako;
    • Eguchi, Mariko;
    • Takada, Yasutsugu
    Publication type:
    Article
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    Revisiting multiple erroneous genetic testing results and clinical misinterpretations in a patient with Li-Fraumeni syndrome: lessons for translational medicine.

    Published in:
    Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-020-00157-8
    By:
    • Sokolova, Tatiana N.;
    • Breder, Valeriy V.;
    • Shumskaya, Irina S.;
    • Suspitsin, Evgeny N.;
    • Aleksakhina, Svetlana N.;
    • Yanus, Grigoriy A.;
    • Tiurin, Vladislav I.;
    • Ivantsov, Alexandr O.;
    • Vona, Barbara;
    • Raskin, Grigoriy A.;
    • Gamajunov, Sergey V.;
    • Imyanitov, Evgeny N.
    Publication type:
    Article