换一批
第一作者：
Fasham, James
作者：
Fasham, James [1]
;
Lin, Siying [2]
;
Ghosh, Promita [3]
;
Radio, Francesca Clementina [4]
;
Farrow, Emily G. [5]
;
Thiffault, Isabelle [6]
;
Kussman, Jennifer [7]
;
Zhou, Dihong [8]
;
Hemming, Rick [9]
;
Zahka, Kenneth [10]
;
Chioza, Barry A. [11]
;
Rawlins, Lettie E. [12]
;
Wenger, Olivia K. [13]
;
Gunning, Adam C. [14]
;
Pizzi, Simone [15]
;
Onesimo, Roberta ;
Zampino, Giuseppe ;
Barker, Emily ;
Osawa, Natasha ;
Rodriguez, Megan Christine ;
Neuhann, Teresa M. ;
Zackai, Elaine H. ;
Keena, Beth ;
Capasso, Jenina ;
Levin, Alex, V ;
Bhoj, Elizabeth ;
Li, Dong ;
Hakonarson, Hakon ;
Wentzensen, Ingrid M. ;
Jackson, Adam ;
Chandler, Kate E. ;
Coban-Akdemir, Zeynep H. ;
Posey, Jennifer E. ;
Banka, Siddharth ;
Lupski, James R. ;
Sheppard, Sarah E. ;
Tartaglia, Marco ;
Triggs-Raine, Barbara ;
Crosby, Andrew H. ;
Baple, Emma L.
作者单位：
Royal Devon & Exeter NHS Fdn Trust,Univ Exeter
[1]
Peninsula Clin Genet Serv,Royal Devon & Exeter NHS Fdn Trust
[2]
Dept Biochem & Med Genet,Univ Manitoba
[3]
Osped Pediat Bambino Gesu,IRCCS
[4]
Genom Med Ctr,Childrens Mercy Hosp
[5]
Pediat Cardiol,Cleveland Clin
[6]
Clin Special Children,New Leaf Ctr
[7]
Ctr Rare Dis & Congenital Defects,Fdn Policlin Univ A Gemelli
[8]
MGZ Med Genet Ctr
[9]
Div Human Genet,Childrens Hosp Philadelphia
[10]
Golisano Childrens Hosp,Univ Rochester
[11]
Ctr Appl Genom,Childrens Hosp Philadelphia
[12]
GeneDx
[13]
St Marys Hosp,Manchester Univ NHS Fdn Trust
[14]
Dept Mol & Human Genet,Baylor Coll Med
[15]
发布时间
2022-07-13
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