檢索結果 - Ingrid Winship

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  1. 1
    Update on Hereditary Colorectal Cancer: Improving the Clinical Utility of Multigene Panel Testing

    Update on Hereditary Colorectal Cancer: Improving the Clinical Utility of Multigene Panel Testing 由 Marie Lorans, Eryn Dow, Finlay Macrae, Ingrid Winship, Daniel D. Buchanan

    出版 2018
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  2. 2
    Women's reflections on fertility and motherhood after breast cancer and its treatment

    Women's reflections on fertility and motherhood after breast cancer and its treatment 由 Maggie Kirkman, Ingrid Winship, C. Stern, Suzanne Neil, G. Bruce Mann, Jane Fisher

    出版 2014
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  3. 3
    Deficiency in Complement Factor B

    Deficiency in Complement Factor B 由 C Slade, Julian J. Bosco, Gary Unglik, Karl Bleasel, Mato Nagel, Ingrid Winship

    出版 2013
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  4. 4
    Mutational analysis of BMP15 and GDF9 as candidate genes for premature ovarian failure

    Mutational analysis of BMP15 and GDF9 as candidate genes for premature ovarian failure 由 Ashwini L. Chand, Anna P. Ponnampalam, Sarah E. Harris, Ingrid Winship, Andrew N. Shelling

    出版 2006
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  5. 5
    Consent Processes for Mobile App Mediated Research: Systematic Review

    Consent Processes for Mobile App Mediated Research: Systematic Review 由 Sarah Moore, Anne-Marie Tassé, Adrian Thorogood, Ingrid Winship, Ma’n H. Zawati, Megan Doerr

    出版 2017
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  6. 6
    Preparing for genomic medicine: a real world demonstration of health system change

    Preparing for genomic medicine: a real world demonstration of health system change 由 Clara Gaff, Ingrid Winship, Susan M. Forrest, David Hansen, Julian Clark, Paul Waring, Mike South, Andrew Sinclair

    出版 2017
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  7. 7
    Loss-of-Function in SMAD4 Might Not Be Critical for Human Natural Killer Cell Responsiveness to TGF-β

    Loss-of-Function in SMAD4 Might Not Be Critical for Human Natural Killer Cell Responsiveness to TGF-β 由 Lachlan Healy, Gustavo Rodrigues Rossi, Jai Rautela, C Slade, Nicholas D. Huntington, Ingrid Winship, Fernando Souza-Fonseca-Guimarães

    出版 2019
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  8. 8
    Evidence for genetic heterogeneity in tuberous sclerosis.

    Evidence for genetic heterogeneity in tuberous sclerosis. 由 Julian R. Sampson, John R.W. Yates, Lindsay A. Pirrit, P Fleury, Ingrid Winship, Peter Beighton, J. M. Connor

    出版 1989
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  9. 9
    Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure

    Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure 由 Wendy J. Watkins, Alexandra J. Umbers, Kathryn J. Woad, Sarah E. Harris, Ingrid Winship, Ksenija Geršak, Andrew N. Shelling

    出版 2006
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  10. 10
    Renal Tumors and Hereditary Pheochromocytoma-Paraganglioma Syndrome Type 4

    Renal Tumors and Hereditary Pheochromocytoma-Paraganglioma Syndrome Type 4 由 Anthony J. Gill, Nicholas Pachter, Adele Clarkson, Katherine Tucker, Ingrid Winship, Diana E. Benn, Bruce G. Robinson, Roderick Clifton‐Bligh

    出版 2011
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  11. 11
    Direct notification by health professionals of relatives at-risk of genetic conditions (with patient consent): views of the Australian public

    Direct notification by health professionals of relatives at-risk of genetic conditions (with patient consent): views of the Australian public 由 Jane Tiller, Ami Stott, Keri Finlay, Tiffany Boughtwood, Evanthia O. Madelli, Ari Horton, Ingrid Winship, Kristen L. Nowak, Margaret Otlowski

    出版 2023
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  12. 12
    Outcomes of a randomised controlled trial of a complex genetic counselling intervention to improve family communication

    Outcomes of a randomised controlled trial of a complex genetic counselling intervention to improve family communication 由 Jan Hodgson, Sylvia A. Metcalfe, Clara Gaff, Susan Donath, Martin B. Delatycki, Ingrid Winship, Loane Skene, MaryAnne Aitken, Jane Halliday

    出版 2015
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  13. 13
    Familial<i>SDHA</i>Mutation Associated With Pituitary Adenoma and Pheochromocytoma/Paraganglioma

    Familial<i>SDHA</i>Mutation Associated With Pituitary Adenoma and Pheochromocytoma/Paraganglioma 由 Trisha Dwight, Kirsty Mann, Diana E. Benn, Bruce G. Robinson, Penny McKelvie, Anthony J. Gill, Ingrid Winship, Roderick Clifton‐Bligh

    出版 2013
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  14. 14
    X-Linked Late-Onset Sensorineural Deafness Caused by a Deletion Involving OA1 and a Novel Gene Containing WD-40 Repeats

    X-Linked Late-Onset Sensorineural Deafness Caused by a Deletion Involving OA1 and a Novel Gene Containing WD-40 Repeats 由 Maria Teresa Bassi, Raj Ramesar, Barbara Caciotti, Ingrid Winship, Alessandro De Grandi, Mirko Riboni, Philip L. Townes, Peter Beighton, Andrea Ballabio, Giuseppe Borsani

    出版 1999
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  15. 15
    Succinate Dehydrogenase Deficiency Is Rare in Pituitary Adenomas

    Succinate Dehydrogenase Deficiency Is Rare in Pituitary Adenomas 由 Anthony J. Gill, Christopher W. Toon, Adele Clarkson, Loretta Sioson, Angela Chou, Ingrid Winship, Bruce G. Robinson, Diana E. Benn, Roderick Clifton‐Bligh, Trisha Dwight

    出版 2014
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  16. 16
    Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review

    Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review 由 Karen E. Wain, Marissa S. Ellingson, Jamie McDonald, Amanda Gammon, Maegan E. Roberts, Pavel N. Pichurin, Ingrid Winship, Douglas L. Riegert‐Johnson, Jeffrey N. Weitzel, Noralane M. Lindor

    出版 2014
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  17. 17
    Inhibin: a candidate gene for premature ovarian failure

    Inhibin: a candidate gene for premature ovarian failure 由 Andrew N. Shelling, Karen A. Burton, Ashwini L. Chand, Cynthia C. van Ee, John T. France, Cindy Farquhar, Stella R. Milsom, Donald R. Love, Ksenija Geršak, Kristiina Aittomäki, Ingrid Winship

    出版 2000
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  18. 18
    Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families

    Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families 由 Zhi L. Teo, Daniel J. Park, Elena Provenzano, Catherine Chatfield, Fabrice Odefrey, Tú Nguyen‐Dumont, James G. Dowty, John L. Hopper, Ingrid Winship, David E. Goldgar, Melissa C. Southey

    出版 2013
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  19. 19
    Community concerns about genetic discrimination in life insurance persist in Australia: A survey of consumers offered genetic testing

    Community concerns about genetic discrimination in life insurance persist in Australia: A survey of consumers offered genetic testing 由 Jane Tiller, Andrew Bakshi, Grace Dowling, Louise Keogh, Aideen M. McInerney‐Leo, Kristine Barlow‐Stewart, Tiffany Boughtwood, Penny Gleeson, Martin B. Delatycki, Ingrid Winship, Margaret Otlowski, Paul Lacaze

    出版 2023
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  20. 20
    Should the grading of colorectal adenocarcinoma include microsatellite instability status?

    Should the grading of colorectal adenocarcinoma include microsatellite instability status? 由 Christophe Rosty, Elizabeth Williamson, Mark Clendenning, Rhiannon Walters, Aung Ko Win, Mark A. Jenkins, John L. Hopper, Ingrid Winship, Melissa C. Southey, Graham G. Giles, Dallas R. English, Daniel D. Buchanan

    出版 2014
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