Corrigendum: High-throughput discovery of novel developmental phenotypes (Nature (2016) 537 (508-514) DOI: 10.1038/nature19356);High-throughput discovery of novel developmental phenotypes

Nature

Volumn 537, Issue 7621, 2016, Pages 508-514

  Dickinson, Mary E ^b   Flenniken, Ann M ^c,d   Ji, Xiao ^e   Teboul, Lydia ^f   Wong, Michael D ^c,u   White, Jacqueline K ^g   Meehan, Terrence F ^g   Weninger, Wolfgang J ^h   Westerberg, Henrik ^f   Adissu, Hibret ^c,u   Baker, Candice N ^a   Bower, Lynette ⁱ   Brown, James M ^f   Brianna Caddle, L ^a   Chiani, Francesco ^j   Clary, Dave ⁱ   Cleak, James ^f   Daly, Mark J ^k,l   Denegre, James M ^a   Doe, Brendan ^g   Dolan, Mary E ^a   Edie, Sarah M ^a   Fuchs, Helmut ^m   Gailus Durner, Valerie ^m   Galli, Antonella ^g   Gambadoro, Alessia ^j   Gallegos, Juan ⁿ   Guo, Shiying ^v   Horner, Neil R ^f   Hsu, Chih wei ^b   Johnson, Sara J ^f   Kalaga, Sowmya ^b   Keith, Lance C ^b   Lanoue, Louise ⁱ   Lawson, Thomas N ^f   Lek, Monkol ^k,l   Mark, Manuel ^o   Marschall, Susan ^m   Mason, Jeremy ^g   McElwee, Melissa L ^b   Newbigging, Susan ^c,u   Nutter, Lauryl M J ^c,u   Peterson, Kevin A ^a   Ramirez Solis, Ramiro ^g   Rowland, Douglas J ⁱ   Ryder, Edward ^g   Samocha, Kaitlin E ^k,l   Seavitt, John R ⁿ   Selloum, Mohammed ^o   Szoke Kovacs, Zsombor ^f   Tamura, Masaru ^p   Trainor, Amanda G ⁱ   Tudose, Ilinca ^g   Wakana, Shigeharu ^p   Warren, Jonathan ^g   Wendling, Olivia ^o   West, David B ^q   Wong, Leeyean ^b   Yoshiki, Atsushi ^p   MacArthur, Daniel G ^k,l   Tocchini Valentini, Glauco P ^j   Gao, Xiang ^v   Flicek, Paul ^g   Bradley, Allan ^g   Skarnes, William C ^g   Justice, Monica J ^n,u   Parkinson, Helen E ^g   Moore, Mark ^w   Wells, Sara ^f   Braun, Robert E ^a   Svenson, Karen L ^a   Hrabe de Angelis, Martin ^m,r,s   Herault, Yann ^o   Mohun, Tim ^t   Mallon, Ann Marie ^f   Mark Henkelman, R ^c,u   Brown, Steve D M ^f   Adams, David J ^g   Kent Lloyd, K C ⁱ   McKerlie, Colin ^c,u   Beaudet, Arthur L ⁿ   Bucan, Maja ^e   Murray, Stephen A ^a   McKay, Matthew ^a   Urban, Barbara ^a   Lund, Caroline ^a   Froeter, Erin ^a   LaCasse, Taylor ^a   Mehalow, Adrienne ^a   Gordon, Emily ^a   Donahue, Leah Rae ^a   Taft, Robert ^a   Kutney, Peter ^a   Dion, Stephanie ^a   Goodwin, Leslie ^a   Kales, Susan ^a   Urban, Rachel ^a   Palmer, Kristina ^a   Pertuy, Fabien ^x   Bitz, Deborah ^x   Weber, Bruno ^x   Goetz Reiner, Patrice ^x   Jacobs, Hughes ^x   Le Marchand, Elise ^x   El Amri, Amal ^x   El Fertak, Leila ^x   Ennah, Hamid ^x   Ali Hadji, Dalila ^x   Ayadi, Abdel ^x   Wattenhofer Donze, Marie ^x   Jacquot, Sylvie ^x   André, Philippe ^x   Birling, Marie Christine ^x   Pavlovic, Guillaume ^x   Sorg, Tania ^x   Morse, Iva ^y   Benso, Frank ^y   Stewart, Michelle E ^z   Copley, Carol ^z   Harrison, Jackie ^z   Joynson, Samantha ^z   Guo, Ruolin ^aa   Qu, Dawei ^aa   Spring, Shoshana ^aa   Yu, Lisa ^aa   Ellegood, Jacob ^aa   Morikawa, Lily ^aa   Shang, Xueyuan ^aa   Feugas, Pat ^aa   Creighton, Amie ^aa   Penton, Patricia Castellanos ^aa   Danisment, Ozge ^aa   Griggs, Nicola ^ab   Tudor, Catherine L ^ab   Green, Angela L ^ab   Icoresi Mazzeo, Cecilia ^ab   Siragher, Emma ^ab   Lillistone, Charlotte ^ab   Tuck, Elizabeth ^ab   Gleeson, Diane ^ab   Sethi, Debarati ^ab   Bayzetinova, Tanya ^ab   Burvill, Jonathan ^ab   Habib, Bishoy ^ab   Weavers, Lauren ^ab   Maswood, Ryea ^ab   Miklejewska, Evelina ^ab   Woods, Michael ^ab   Grau, Evelyn ^ab   Newman, Stuart ^ab   Sinclair, Caroline ^ab   Brown, Ellen ^ab   Ayabe, Shinya ^p   Iwama, Mizuho ^p   Murakami, Ayumi ^p   more..

^a JACKSON LABORATORY   (United States)

^b Department of Molecular Physiology and Biophysics ^*  (United States)

^c Centre for Phenogenomics (TCP)   (Canada)

^d MOUNT SINAI HOSPITAL   (Canada)

^e UNIVERSITY OF PENNSYLVANIA   (United States)

^f MRC MAMMALIAN GENETICS UNIT   (United Kingdom)

^g WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^h MEDICAL UNIVERSITY OF VIENNA   (Austria)

ⁱ UNIVERSITY OF CALIFORNIA   (United States)

^j CNR   (Italy)

^k MASSACHUSETTS GENERAL HOSPITAL   (United States)

^l BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^m INSTITUTE OF EPIDEMIOLOGY   (Germany)

ⁿ BAYLOR COLLEGE OF MEDICINE   (United States)

^o INSTITUT CLINIQUE DE LA SOURIS   (France)

^p RIKEN BIORESOURCE CENTER   (Japan)

^q CHILDREN S HOSPITAL OAKLAND RESEARCH INSTITUTE   (United States)

^r TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^s GERMAN CENTER FOR DIABETES RESEARCH DZD   (Germany)

^t THE FRANCIS CRICK INSTITUTE   (United Kingdom)

^u HOSPITAL FOR SICK CHILDREN   (Canada)

^v NANJING UNIVERSITY   (China)

^w IMPC   (United States)

^x Institut Clinique de la Souris (ICS)   (United States)

^y CHARLES RIVER LABORATORIES   (United States)

^z MRC Harwell   (United Kingdom)

^aa Toronto Centre for Phenogenomics   (Canada)

^ab WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

BETA GALACTOSIDASE;

DISEASE INCIDENCE; GENE EXPRESSION; GENETIC ANALYSIS; MUTATION; PHENOTYPE; RODENT;

ALLELE; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BICUSPID AORTIC VALVE; BLEEDING; CEREBELLUM HYPOPLASIA; CILIARY DYSKINESIA; CONTROLLED STUDY; CRANIOFACIAL MALFORMATION; CYCLOPIA; DEVELOPMENTAL DISORDER; EDEMA; EMBRYO; EMBRYO DEATH; ESSENTIAL GENE; EXENCEPHALY; GENE CASSETTE; GENE EXPRESSION; GENE FUNCTION; GENE MUTATION; GENETIC ANALYSIS; GENETIC BACKGROUND; GENOME-WIDE ASSOCIATION STUDY; GERM LINE; HETEROZYGOTE; HIGH THROUGHPUT SEQUENCING; HOLOPROSENCEPHALY; HUMAN; HUMAN CELL; HYDROCEPHALUS; LETHAL GENE; MOUSE; MUTANT; NEURAL TUBE DEFECT; NONHUMAN; NULL ALLELE; PENETRANCE; PHENOTYPE; POLYDACTYLY; PRIORITY JOURNAL; SPINAL DYSRAPHISM; ANIMAL; C57BL MOUSE; CONSERVED SEQUENCE; DISEASES; EMBRYOLOGY; GENETICS; HIGH THROUGHPUT SCREENING; KNOCKOUT MOUSE; MAMMALIAN EMBRYO; METABOLISM; MUTATION; SEQUENCE HOMOLOGY; SINGLE NUCLEOTIDE POLYMORPHISM; THREE DIMENSIONAL IMAGING;

MAMMALIA; MUS;

ANIMALS; CONSERVED SEQUENCE; DISEASE; EMBRYO, MAMMALIAN; GENES, ESSENTIAL; GENES, LETHAL; GENOME-WIDE ASSOCIATION STUDY; HIGH-THROUGHPUT SCREENING ASSAYS; HUMANS; IMAGING, THREE-DIMENSIONAL; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MUTATION; PENETRANCE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE HOMOLOGY;

EID: 84989204804     PISSN: 00280836     EISSN: 14764687     Source Type: Journal    
DOI: 10.1038/nature24643     Document Type: Erratum

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