作者：
Ghali, Neeti [1]
;
Baker, Duncan [2]
;
Brady, Angela F. [3]
;
Burrows, Nigel [4]
;
Cervi, Elena [5]
;
Cilliers, Deirdre [6]
;
Frank, Michael [7]
;
Germain, Dominique P. [8]
;
Hulmes, David J. S. [9]
;
Jacquemont, Marie-line [10]
;
Kannu, Peter [11]
;
Lefroy, Henrietta [12]
;
Legrand, Anne [13]
;
Pope, F. Michael [14]
;
Robertson, Lisa [15]
;
Vandersteen, Anthony [16]
;
von Klemperer, Kate ;
Warburton, Renarta ;
Whiteford, Margo ;
van Dijk, Fleur S.
作者单位：
London North West Healthcare Univ NHS Trust, Ehlers Danlos Syndrome Natl Diagnost Serv London
[1]
Great Ormond St Hosp NHS Fdn Trust, Ctr Inherited Cardiovasc Dis, London, England
[2]
Cambridge Univ Hosp NHS Fdn Trust, Dept Dermatol, Cambridge, England
[3]
Hop Europeen Georges Pompidou, AP HP, Ctr Reference Malad Vasculaires Rares, Paris, France
[4]
Queen Elizabeth Univ Hosp Glasgow, Clin Genet West Scotland Reg Genet Serv, Glasgow, Lanark
[5]
Paris Saclay Univ, Univ Versailles, Div Med Genet, Montigny, France
[6]
Hosp Sick Children, Div Clin & Metab Genet, Toronto, ON, Canada
[7]
Connect Tissue Disorders Serv, Sheffield Diagnost Genet Serv, Sheffield, S Yorkshire, England
[8]
Oxford Univ NHS Fdn Trust, Oxford Ctr Genom Med, Oxford, England
[9]
CHU La Reunion, Med Genet Unit, St Pierre, St Pierre & Miq, France
[10]
Chelsea & Westminster Hosp NHS Fdn Trust, Dept Dermatol, London, England
[11]
IWK Hlth Ctr, Maritime Med Genet Serv, Halifax, NS, Canada
[12]
St Barthlomews Hosp, Dept Cardiol, London, England
[13]
Univ Claude Bernard Lyon 1, CNRS, UMR5305, Lyon, France
[14]
Hop Europ Georges Pompidou, AP HP, Dept Genet, Paris, France
[15]
Aberdeen Royal Infirm, Dept Clin Genet, Aberdeen, Scotland
[16]
发布时间
2020-11-17
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