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Author/Creator Renner, Stefan P

1. High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia. Issue 3 (28th January 2011)

Authors:
Nik-Zainal, Serena; Strick, Reiner; Storer, Mekayla; Huang, Ni; Rad, Roland; Willatt, Lionel; Fitzgerald, Tomas; Martin, Vicki; Sandford, Richard; Carter, Nigel P; Janecke, Andreas R; Renner, Stefan P; Oppelt, Patricia G; Oppelt, Peter; Schulze, Christine; Brucker, Sara; Hurles, Matthew; Beckmann...
Journal:
Journal of medical genetics
Issue:
Volume 48:Issue 3(2011)
Page Start:
197
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS. Issue 12 (5th September 2016)

Authors:
Southey, Melissa C; Goldgar, David E; Winqvist, Robert; Pylkäs, Katri; Couch, Fergus; Tischkowitz, Marc; Foulkes, William D; Dennis, Joe; Michailidou, Kyriaki; van Rensburg, Elizabeth J; Heikkinen, Tuomas; Nevanlinna, Heli; Hopper, John L; Dörk, Thilo; Claes, Kathleen BM; Reis-Filho, Jorge; Teo, ...
Journal:
Journal of medical genetics
Issue:
Volume 53:Issue 12(2016)
Page Start:
800
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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