作者单位：
IMAGINE Inst, INSERM, UMR1163, Paris, France
[1]
CHI Poissy, Dept Genet, Reference Ctr Rare Dev Dis AnD DI Rares, Poissy, France
[2]
Hop Necker Enfants Malad, AP HP, Unite Embryofoetopathol, Serv Histol Embryol Cytogenet, Paris
[3]
Univ Paris 05, Dept Genet, Sorbonne Paris Cite, Paris, France
[4]
Necker Enfants Malad Hosp, AP HP, Reference Ctr Skeletal Dysplasia, Paris, France
[5]
发布时间
2020-09-02
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