作者：
Carrieri, Daniele [1]
;
Howard, Heidi C. [2]
;
Benjamin, Caroline [3]
;
Clarke, Angus J. [4]
;
Dheensa, Sandi [5]
;
Doheny, Shane [6]
;
Hawkins, Naomi [7]
;
Halbersma-Konings, Tanya F. [8]
;
Jackson, Leigh [9]
;
Kayserili, Hulya [10]
;
Kelly, Susan E. [11]
;
Lucassen, Anneke M. [12]
;
Mendes, Alvaro [13]
;
Rial-Sebbag, Emmanuelle [14]
;
Stefansdottir, Vigdis [15]
;
Turnpenny, Peter D. ;
van El, Carla G. ;
van Langen, Irene M. ;
Cornel, Martina C. ;
Forzano, Francesca
作者单位：
Royal Devon & Exeter NHS Fdn Trust, Clin Genet, Exeter, Devon, England
[1]
Univ Exeter, Sch Med, Egenis, England
[2]
Univ Cent Lancashire UCLan, Sch Community Hlth & Midwifery, Preston, Lancs, England
[3]
Natl Univ Hosp Iceland, Dept Genet & Mol Med, Landspitali, Reykjavik, Iceland
[4]
Univ Porto, I3S, IBMC Inst Mol & Cell Biol, UnIGENe, Porto, Portugal
[5]
Univ Paul Sabatier Toulouse III, INSERM, UMR 1027, Toulouse, France
[6]
Univ Southampton, Fac Med, Clin Eth & Law, Southampton, Hants, England
[7]
Vrije Univ, Amsterdam UMC, Sect Community Genet, Dept Clin Genet, Amsterdam, Netherlands
[8]
Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands
[9]
Koc Univ KUSoM, Sch Med, Med Genet Dept, Istanbul, Turkey
[10]
Uppsala Univ, Ctr Res Eth & Bioeth, Uppsala, Sweden
[11]
Univ Exeter, Law Sch, Exeter, Devon, England
[12]
Univ Exeter, Egenis, England
[13]
Guys & St Thomas NHS Fdn Trust, Clin Genet Dept, London, ON, Canada
[14]
Cardiff Univ, Sch Med, Cardiff, S Glam, Wales
[15]
发布时间
2019-09-17
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