作者：
Vilboux, Thierry [1]
;
Doherty, Daniel A. [2]
;
Glass, Ian A. [3]
;
Parisi, Melissa A. [4]
;
Phelps, Ian G. [5]
;
Cullinane, Andrew R. [6]
;
Zein, Wadih [7]
;
Brooks, Brian P. [8]
;
Heller, Theo ;
Soldatos, Ariane ;
Oden, Neal L. ;
Yildirimli, Deniz ;
Vemulapalli, Meghana ;
Mullikin, James C. ;
Malicdan, May Christine V. ;
Gahl, William A. ;
Gunay-Aygun, Meral
作者单位：
Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[1]
NIH, Undiagnosed Dis Program Common Fund, Bethesda, MD USA
[2]
Natl Inst Diabet & Digest & Kidney Dis, Liver Dis Branch, Bethesda, MD USA
[3]
Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, NIH, Bethesda, MD USA
[4]
NHGRI, NIH, Med Genet Branch, Bethesda, MD USA
[5]
EMMES Corp, Rockville, MD USA
[6]
NHGRI, NIH, Intramural Sequencing Ctr, Bethesda, MD USA
[7]
NEI, NIH, Ophthalm Genet & Visual Funct Branch, Bethesda, MD USA
[8]
发布时间
2018-02-04
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