Showing 1–9 of 9 results
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A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment
- Nanna D Rendtorff
- , Mei Zhu
- , Toril Fagerheim
- , Torben L Antal
- , MaryPat Jones
- , Tanya M Teslovich
- , Elizabeth M Gillanders
- , Michael Barmada
- , Erik Teig
- , Jeffrey M Trent
- , Karen H Friderici
- , Dietrich A Stephan
- & Lisbeth Tranebjærg
European Journal of Human Genetics 14 , 1097–1105 -
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Common sequence variants on 20q11.22 confer melanoma susceptibility
- Kevin M Brown
- , Stuart MacGregor
- , Grant W Montgomery
- , David W Craig
- , Zhen Zhen Zhao
- , Kelly Iyadurai
- , Anjali K Henders
- , Nils Homer
- , Megan J Campbell
- , Mitchell Stark
- , Shane Thomas
- , Helen Schmid
- , Elizabeth A Holland
- , Elizabeth M Gillanders
- , David L Duffy
- , Judith A Maskiell
- , Jodie Jetann
- , Megan Ferguson
- , Dietrich A Stephan
- , Anne E Cust
- , David Whiteman
- , Adele Green
- , Håkan Olsson
- , Susana Puig
- , Paola Ghiorzo
- , Johan Hansson
- , Florence Demenais
- , Alisa M Goldstein
- , Nelleke A Gruis
- , David E Elder
- , Julia Newton Bishop
- , Richard F Kefford
- , Graham G Giles
- , Bruce K Armstrong
- , Joanne F Aitken
- , John L Hopper
- , Nicholas G Martin
- , Jeffrey M Trent
- , Graham J Mann
- & Nicholas K Hayward
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