作者：
Bonafe, Luisa [1]
;
Cormier-Daire, Valerie [2]
;
Hall, Christine [3]
;
Lachman, Ralph [4]
;
Mortier, Geert [5]
;
Mundlos, Stefan [6]
;
Nishimura, Gen [7]
;
Sangiorgi, Luca [8]
;
Savarirayan, Ravi [9]
;
Sillence, David [10]
;
Spranger, Juergen [11]
;
Superti-Furga, Andrea [12]
;
Warman, Matthew [13]
;
Unger, Sheila
作者单位：
Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany
[1]
Tokyo Metropolitan Childrens Med Ctr, Dept Radiol, Tokyo, Japan
[2]
IRCCS Rizzoli Orthopaed Inst IOR, Dept Med Genet & Skeletal Rare Dis, Bologna, Italy
[3]
Univ Lausanne, CHUV, Dept Pediat, CH-1011 Lausanne, Switzerland
[4]
Univ Calif Los Angeles, Int Skeletal Dysplasia Registry, Los Angeles, CA USA
[5]
Murdoch Childrens Res Inst, Parkville, Vic, Australia
[6]
Boston Childrens Hosp, Orthopaed Res Labs, Boston, MA USA
[7]
Univ Lausanne, Ctr Malad Mol CHUV, CH-1011 Lausanne, Switzerland
[8]
Univ Sydney, Childrens Hosp Westmead, Sydney Med Sch, Sch Clin,Discipline Genet Med,Head Connect
[9]
Univ Lausanne, CHUV, Med Genet Serv, CH-1011 Lausanne, Switzerland
[10]
Great Ormond St Hosp Sick Children, Dept Radiol, London, England
[11]
Univ Antwerp, Fac Med & Hlth Sci, Dept Med Genet, B-2020 Antwerp, Belgium
[12]
Hop Necker Enfants Malad, IMAGINE Inst, Paris, France
[13]
发布时间
2017-04-05
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