نتائج البحث - Marc Tischkowitz
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PALB2/FANCN: Recombining Cancer and Fanconi Anemia حسب Marc Tischkowitz, Bing Xia
منشور في 2010Revisão -
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Fanconi anaemia,<i>BRCA2</i>mutations and childhood cancer: a developmental perspective from clinical and epidemiological observations with implications for genetic counselling حسب Stefan Meyer, Marc Tischkowitz, Kate Chandler, Alan Gillespie, Jillian M. Birch, D. Gareth Evans
منشور في 2013Revisão -
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Consensus for genes to be included on cancer panel tests offered by UK genetics services: guidelines of the UK Cancer Genetics Group حسب Amy Taylor, Angela F. Brady, Ian M. Frayling, Helen Hanson, Marc Tischkowitz, Clare Turnbull, Lucy Side
منشور في 2018Artigo -
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p.Val804Met, the Most Frequent Pathogenic Mutation in RET, Confers a Very Low Lifetime Risk of Medullary Thyroid Cancer حسب Chey Loveday, Katherine Josephs, Daniel Chubb, Adam C. Gunning, Louise Izatt, Marc Tischkowitz, Sian Ellard, Clare Turnbull
منشور في 2018Artigo -
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Pathology update to the Manchester Scoring System based on testing in over 4000 families حسب D. Gareth Evans, Elaine F. Harkness, Inga Plaskocinska, Andrew Wallace, Tara Clancy, Emma R. Woodward, Anthony Howell, Marc Tischkowitz, Fiona Lalloo
منشور في 2017Artigo -
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Long-term outcomes of hysterectomy with bilateral salpingo-oophorectomy: a systematic review and meta-analysis حسب Hend Hassan, Isaac Allen, Eleni Sofianopoulou, Yvonne Walburga, Clare Turnbull, Diana Eccles, Marc Tischkowitz, Paul D.P. Pharoah, Antonis C. Antoniou
منشور في 2023Revisão -
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UKCGG Consensus Group guidelines for the management of patients with constitutional <i>TP53</i> pathogenic variants حسب Helen Hanson, Angela F. Brady, Gillian Crawford, Rosalind A. Eeles, S. L. Gibson, Mette Jorgensen, Louise Izatt, Aslam Sohaib, Marc Tischkowitz, D. Gareth Evans
منشور في 2020Artigo -
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Endoscopic surveillance with systematic random biopsy for the early diagnosis of hereditary diffuse gastric cancer: a prospective 16-year longitudinal cohort study حسب Colin Y. C. Lee, Adriaan Olivier, Judith Honing, Anne Lydon, Susan Richardson, Maria O’Donovan, Marc Tischkowitz, Rebecca C. Fitzgerald, Massimiliano di Pietro
منشور في 2022Artigo -
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Use of immunohistochemical markers can refine prognosis in triple negative breast cancer حسب Marc Tischkowitz, Jean‐Sébastien Brunet, Louis R. Bégin, David G. Huntsman, Maggie C.U. Cheang, Lars A. Akslen, Torsten O. Nielsen, William D. Foulkes
منشور في 2007Artigo -
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Analysis of the Gene Coding for the BRCA2-Interacting Protein PALB2 in Familial and Sporadic Pancreatic Cancer حسب Marc Tischkowitz, Nelly Sabbaghian, Nancy Hamel, Ayelet Borgida, Chaim Rosner, Nassim Taherian, Archana Srivastava, Spring Holter, Heidi Rothenmund, Parviz Ghadirian, William D. Foulkes, Steven Gallinger
منشور في 2009Carta -
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Management of individuals with germline variants in PALB2: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG) حسب Marc Tischkowitz, Judith Balmañà, William D. Foulkes, Paul A. James, Joanne Ngeow, Rita K. Schmutzler, Nicoleta Voian, Myra J. Wick, Douglas R. Stewart, Tuya Pal
منشور في 2021Artigo -
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Cancer and Overgrowth Manifestations of PTEN Hamartoma Tumour Syndrome: Management Recommendations from the International PHTS Consensus Guidelines Working Group حسب Andrew Dhawan, Sarah Baitamouni, Darren Liu, Lamis Yehia, Kristin Anthony, Alicia McCarther, Marc Tischkowitz, Suzanne P. MacFarland, Joanne Ngeow, Nicoline Hoogerbrugge, Charis Eng
منشور في 2025Artigo -
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Serum levels of mature microRNAs in DICER1-mutated pleuropulmonary blastoma حسب Matthew J. Murray, Shivani Bailey, Katie L. Raby, Harpreet K. Saini, Leanne de Kock, G.A. Amos Burke, William D. Foulkes, Anton J. Enright, Nicholas Coleman, Marc Tischkowitz
منشور في 2014Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Medicine
Cancer
Genetics
Gene
Internal medicine
Oncology
Mutation
Breast cancer
Germline mutation
Cancer research
Gynecology
Ovarian cancer
PALB2
Computer science
Environmental health
Germline
Phenotype
Population
Pathology
Family history
Genetic testing
Allele
Computational biology
Exome sequencing
Family medicine
BRCA2 Protein
Bioinformatics
Genotype
Missense mutation