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Author/Creator Carter, Nigel P

1. Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data. Issue 9975 (4th April 2015)

Authors:
Wright, Caroline F; Fitzgerald, Tomas W; Jones, Wendy D; Clayton, Stephen; McRae, Jeremy F; van Kogelenberg, Margriet; King, Daniel A; Ambridge, Kirsty; Barrett, Daniel M; Bayzetinova, Tanya; Bevan, A Paul; Bragin, Eugene; Chatzimichali, Eleni A; Gribble, Susan; Jones, Philip; Krishnappa, Netrava...
Journal:
Lancet
Issue:
Volume 385:Issue 9975(2015)
Page Start:
1305
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data. Issue 9975 (4th April 2015)

Authors:
Wright, Caroline F; Fitzgerald, Tomas W; Jones, Wendy D; Clayton, Stephen; McRae, Jeremy F; van Kogelenberg, Margriet; King, Daniel A; Ambridge, Kirsty; Barrett, Daniel M; Bayzetinova, Tanya; Bevan, A Paul; Bragin, Eugene; Chatzimichali, Eleni A; Gribble, Susan; Jones, Philip; Krishnappa, Netrava...
Journal:
Lancet
Issue:
Volume 385:Issue 9975(2015)
Page Start:
1305
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. 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
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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