A 3.7 Mb Deletion Encompassing ZEB2 Causes a Novel Polled and Multisystemic Syndrome in the Progeny of a Somatic Mosaic Bull

PLoS ONE

Volumn 7, Issue 11, 2012, Pages

  Capitan, Aurélien ^a,b   Allais Bonnet, Aurélie ^c   Pinton, Alain ^d   Marquant Le Guienne, Brigitte ^e   Le Bourhis, Daniel ^c,e   Grohs, Cécile ^a   Bouet, Stéphan ^a   Clément, Laëtitia ^e   Salas Cortes, Laura ^e   Venot, Eric ^a   Chaffaux, Stéphane ^a   Weiss, Bernard ^a   Delpeuch, Arnaud ^f   Noé, Guy ^g   Rossignol, Marie Noëlle ^g   Barbey, Sarah ^h   Dozias, Dominique ^h   Cobo, Emilie ^h   Barasc, Harmonie ^d   Auguste, Aurélie ^c   Pannetier, Maëlle ^c   Deloche, Marie Christine ^e   Lhuilier, Emeline ^h,i   Bouchez, Olivier ^h,i   Esquerré, Diane ^h,i   Salin, Gérald ^h,i   Klopp, Christophe ^h   Donnadieu, Cécile ^h,i   Chantry Darmon, Céline ^g   Hayes, Hélène ^a   Gallard, Yves ^h   Ponsart, Claire ^e   Boichard, Didier ^a   Pailhoux, Eric ^c   more..

^a UMR1313 GÉNÉTIQUE ANIMALE ET BIOLOGIE INTÉGRATIVE   (France)

^b UNCEIA   (France)

^c INRA Institut National de la Recherche Agronomique   (France)

^d CNRS   (France)

^e UNCEIA Union Nationale des Cooperatives d'Elevage et d'Insemination Animale   (France)

^f Institut de l'Elevage   (France)

^g LABOGENA   (France)

^h CEMAGREF   (France)

ⁱ GeT PlaGe Genotoul   (France)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR ZEB2; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARHGAP15 GENE; ARTICLE; AUTOSOME MOSAICISM; BULL (BOVINE); CHROMOSOME DELETION; CLINICAL FEATURE; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; EMBRYO; EPITHELIAL MESENCHYMAL TRANSITION; FEMALE; FETUS; GENE; GENE DELETION; GENE EXPRESSION; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC DISORDER; GENOME ANALYSIS; GLYCOSYLTRANSFERASE LIKE DOMAIN CONTAINING 1 GENE; HETEROZYGOSITY LOSS; HISTOPATHOLOGY; HUMAN; LETHALITY; MALE; MOWAT WILSON SYNDROME; NONHUMAN; ONTOGENY; PATHOGENICITY; POLLED AND MULTISYSTEMIC SYNDROME; PROGENY; ZINC FINGER E BOX BINDING HOMEOBOX 2 GENE;

ABNORMALITIES, MULTIPLE; ANIMALS; BASE PAIRING; CATTLE; CATTLE DISEASES; CHROMOSOME MAPPING; FEMALE; FETUS; HORNS; HUMANS; INHERITANCE PATTERNS; MALE; MOSAICISM; MUTATION; PREGNANCY; REAL-TIME POLYMERASE CHAIN REACTION; REPRESSOR PROTEINS; SEQUENCE DELETION; SKIN; SYNDROME;

ANIMALIA; BOVIDAE; BOVINAE; MAMMALIA; MURINAE;

EID: 84869074293     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0049084     Document Type: Article

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