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Clinical evidence for a mandibular to maxillary transformation in Auriculocondylar syndrome

dc.contributor.authorGordon, Christopher T.en_US
dc.contributor.authorCunniff, Christopher M.en_US
dc.contributor.authorGreen, Glenn E.en_US
dc.contributor.authorZechi‐ceide, Roseli Mariaen_US
dc.contributor.authorJohnson, Jason M.en_US
dc.contributor.authorHenderson, Alexen_US
dc.contributor.authorPetit, Florenceen_US
dc.contributor.authorKokitsu‐nakata, Nancy Mizueen_US
dc.contributor.authorGuion‐almeida, Maria Leineen_US
dc.contributor.authorMunnich, Arnolden_US
dc.contributor.authorCunningham, Michael L.en_US
dc.contributor.authorLyonnet, Stanislasen_US
dc.contributor.authorAmiel, Jeanneen_US
dc.date.accessioned2014-07-03T14:41:15Z
dc.date.availableWITHHELD_13_MONTHSen_US
dc.date.available2014-07-03T14:41:15Z
dc.date.issued2014-07en_US
dc.identifier.citationGordon, Christopher T.; Cunniff, Christopher M.; Green, Glenn E.; Zechi‐ceide, Roseli Maria ; Johnson, Jason M.; Henderson, Alex; Petit, Florence; Kokitsu‐nakata, Nancy Mizue ; Guion‐almeida, Maria Leine ; Munnich, Arnold; Cunningham, Michael L.; Lyonnet, Stanislas; Amiel, Jeanne (2014). "Clinical evidence for a mandibular to maxillary transformation in Auriculocondylar syndrome." American Journal of Medical Genetics Part A 164(7): 1850-1853.en_US
dc.identifier.issn1552-4825en_US
dc.identifier.issn1552-4833en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/107487
dc.publisherWiley Periodicals, Inc.en_US
dc.titleClinical evidence for a mandibular to maxillary transformation in Auriculocondylar syndromeen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/107487/1/ajmga36505.pdf
dc.identifier.doi10.1002/ajmg.a.36505en_US
dc.identifier.sourceAmerican Journal of Medical Genetics Part Aen_US
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dc.identifier.citedreferenceGordon CT, Vuillot A, Marlin S, Gerkes E, Henderson A, Alkindy A, Holder‐Espinasse M, Park SS, Omarjee A, Sanchis‐Borja M, Bdira EB, Oufadem M, Sikkema‐Raddatz B, Stewart A, Palmer R, McGowan R, Petit F, Delobel B, Speicher MR, Aurora P, Kilner D, Pellerin P, Simon M, Bonnefont JP, Tobias ES, Garcia‐Minaur S, Bitner‐Glindzicz M, Lindholm P, Meijer BA, Abadie V, Denoyelle F, Vazquez MP, Rotky‐Fast C, Couloigner V, Pierrot S, Manach Y, Breton S, Hendriks YM, Munnich A, Jakobsen L, Kroisel P, Lin A, Kaban LB, Basel‐Vanagaite L, Wilson L, Cunningham ML, Lyonnet S, Amiel J. 2013. Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome. J Med Genet 50: 174 – 186.en_US
dc.identifier.citedreferenceGuion‐Almeida ML, Zechi‐Ceide RM, Vendramini S, Kokitsu‐Nakata NM. 2002. Auriculo‐condylar syndrome: Additional patients. Am J Med Genet 112: 209 – 214.en_US
dc.identifier.citedreferenceMasotti C, Oliveira KG, Poerner F, Splendore A, Souza J, Freitas Rda S, Zechi‐Ceide R, Guion‐Almeida ML, Passos‐Bueno MR. 2008. Auriculo‐condylar syndrome: Mapping of a first locus and evidence for genetic heterogeneity. Eur J Hum Genet 16: 145 – 152.en_US
dc.identifier.citedreferenceOzeki H, Kurihara Y, Tonami K, Watatani S, Kurihara H. 2004. Endothelin‐1 regulates the dorsoventral branchial arch patterning in mice. Mech Dev 121: 387 – 395.en_US
dc.identifier.citedreferenceRieder MJ, Green GE, Park SS, Stamper BD, Gordon CT, Johnson JM, Cunniff CM, Smith JD, Emery SB, Lyonnet S, Amiel J, Holder M, Heggie AA, Bamshad MJ, Nickerson DA, Cox TC, Hing AV, Horst JA, Cunningham ML. 2012. A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome. Am J Hum Genet 90: 907 – 914.en_US
dc.identifier.citedreferenceRuest LB, Xiang X, Lim KC, Levi G, Clouthier DE. 2004. Endothelin‐A receptor‐dependent and ‐independent signaling pathways in establishing mandibular identity. Development 131: 4413 – 4423.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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