换一批Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype
第一作者：
Hiatt, Susan M.
作者：
Hiatt, Susan M. [1]
;
Trajkova, Slavica [2]
;
Sebastiano, Matteo Rossi [3]
;
Partridge, E. Christopher [4]
;
Abidi, Fatima E. [5]
;
Anderson, Ashlyn [6]
;
Ansar, Muhammad [7]
;
Antonarakis, Stylianos E. [8]
;
Azadi, Azadeh [9]
;
Bachmann-Gagescu, Ruxandra [10]
;
Bartuli, Andrea [11]
;
Benech, Caroline [12]
;
Berkowitz, Jennifer L. [13]
;
Betti, Michael J. [14]
;
Brusco, Alfredo [15]
;
Cannon, Ashley [16]
;
Caron, Giulia [17]
;
Chen, Yanmin [18]
;
Cochran, Meagan E. [19]
;
Coleman, Tanner F. [20]
;
Crenshaw, Molly M. [21]
;
Cuisset, Laurence [22]
;
Curry, Cynthia J. [23]
;
Darvish, Hossein [24]
;
Demirdas, Serwet [25]
;
Descartes, Maria [26]
;
Douglas, Jessica [27]
;
Dyment, David A. [28]
;
Elloumi, Houda Zghal [29]
;
Ermondi, Giuseppe [30]
;
Faoucher, Marie [31]
;
Farrow, Emily G. [32]
;
Felker, Stephanie A. [33]
;
Fisher, Heather [34]
;
Hurst, Anna C. E. [35]
;
Joset, Pascal [36]
;
Kelly, Melissa A. [37]
;
Kmoch, Stanislav [38]
;
Leadem, Benjamin R. [39]
;
Lyons, Michael J. [40]
;
Macchiaiolo, Marina [41]
;
Magner, Martin [42]
;
Mandrile, Giorgia ;
Mattioli, Francesca ;
McEown, Megan ;
Meadows, Sarah K. ;
Medne, Livija ;
Meeks, Naomi J. L. ;
Montgomery, Sarah ;
Napier, Melanie P. ;
Natowicz, Marvin ;
Newberry, Kimberly M. ;
Niceta, Marcello ;
Noskova, Lenka ;
Nowak, Catherine B. ;
Noyes, Amanda G. ;
Osmond, Matthew ;
Prijoles, Eloise J. ;
Pugh, Jada ;
Pullano, Verdiana ;
Quelin, Chloe ;
Rahimi-Aliabadi, Simin ;
Rauch, Anita ;
Redon, Sylvia ;
Reymond, Alexandre ;
Schwager, Caitlin R. ;
Sellars, Elizabeth A. ;
Scheuerle, Angela E. ;
Shukarova-Angelovska, Elena ;
Skraban, Cara ;
Stolerman, Elliot ;
Sullivan, Bonnie R. ;
Tartaglia, Marco ;
Thiffault, Isabelle ;
Uguen, Kevin ;
Umana, Luis A. ;
Bever, Yolande van ;
Crabben, Saskia N. van der ;
Slegtenhorst, Marjon A. van ;
Waisfisz, Quinten ;
Washington, Camerun ;
Rodan, Lance H. ;
Myers, Richard M. ;
Cooper, Gregory M.
作者单位：
Mol Biotechnol & Hlth Sci Dept,Univ Torino
[1]
Greenwood Genet Ctr
[2]
Jules Gonin Eye Hosp,Univ Lausanne
[3]
Dept Genet Med & Dev,Univ Geneva
[4]
Dept Med Sci,Univ Torino
[5]
Obestetr & Gynecol Dept,Golestan Univ Med Sci
[6]
Ctr Pediat Genom Med,Childrens Mercy Kansas City
[7]
Vanderbilt Univ Sch Med
[8]
Childrens Med Ctr
[9]
Inst Med Genet & Pathol,Univ Hosp Basel
[10]
HudsonAlpha Clin Serv Lab LLC
[11]
Hudson Alpha Inst Biotechnol
[12]
Amsterdam Neurosci
[13]
Inst Med Genet,Univ Zurich
[14]
Osped Pediatr Bambino Gesu,IRCCS
[15]
Inserm,Univ Brest
[16]
GeneDx LLC
[17]
Fac Med 1,Charles Univ Prague
[18]
Gen Univ Hosp,Charles Univ Prague
[19]
San Luigi Univ Hosp,Univ Torino
[20]
Childrens Hosp Philadelphia
[21]
Dept Pediat,Univ Colorado
[22]
Ctr Integrat Genom,Univ Lausanne
[23]
Dept Clin Genet,Erasmus MC Univ Med Ctr
[24]
Dept Genet,Univ Alabama Birmingham
[25]
Pediat & Med Genet,Univ Colorado
[26]
Hop Cochin,Univ Paris Cite
[27]
Genet Med,UCSF Fresno
[28]
Nikagene Genet Diag Lab
[29]
Boston Childrens Hosp
[30]
Childrens Hosp Eastern Ontario Res Inst
[31]
CNRS,Univ Rennes
[32]
Genom Med Neurol & Pediat Inst,Cleveland Clin
[33]
Ctr Reference Malad Rares CLAD Ouest,CHU Hop Sud
[34]
Coll Pharm,Univ Utah
[35]
Univ Childrens Hosp Zurich,Univ Zurich
[36]
Ctr Reference Deficiences Intellectuelles causes r
[37]
Div Genet,Childrens Mercy Kansas City
[38]
Genet & Metab,Arkansas Childrens Hosp
[39]
Dept Pediat,Univ Texas Southwestern Med Ctr
[40]
Univ Clin Childrens Dis,Univ Sv Kiril & Metodij
[41]
Dept Clin Genet,Amsterdam Univ Med Ctr
[42]
发布时间
2023-06-13
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The American Journal of Human Genetics
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