Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12104/71328
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dc.contributor.authorBecerra-Solano, L.E.
dc.contributor.authorDiaz-Rodriguez, M.
dc.contributor.authorNastasi-Catanese, J.A.
dc.contributor.authorToscano-Flores, J.J.
dc.contributor.authorBanuelos-Robles, O.
dc.contributor.authorFiguera, L.E.
dc.contributor.authorMatute, E.
dc.contributor.authorDe Lourdes Ramirez-Duenas, M.
dc.date.accessioned2015-11-19T18:57:53Z-
dc.date.available2015-11-19T18:57:53Z-
dc.date.issued2008
dc.identifier.urihttp://hdl.handle.net/20.500.12104/71328-
dc.description.abstractWe report the fifth female patient with Myhre syndrome (MS) and review the literature. She is a 13-year-old Mexican girl whose phenotype fulfills all the clinical and radiological criteria reported in MS such as typical facies, short stature, limited joint mobility, and short hands and feet. The physical habitus of MS is described and a square body shape is clearly distinguished in all cases. As the typical muscular build is present mainly in male patients, the MS muscular appearance may be hormonally influenced. © 2008 Lippincott Williams & Wilkins, Inc.
dc.titleThe fifth female patient with Myhre syndrome: Further delineation
dc.typeArticle
dc.identifier.doi10.1097/MCD.0b013e3282f52828
dc.relation.ispartofjournalClinical Dysmorphology
dc.relation.ispartofvolume17
dc.relation.ispartofissue2
dc.relation.ispartofpage113
dc.relation.ispartofpage117
dc.subject.keywordBlepharophimosis; Cleft palate; Myhre syndrome; Precocious puberty
dc.contributor.affiliationBecerra-Solano, L.E., Genetics Division, Biomedical Research Center, West-Mexican Social Security Institute, Guadalajara, Mexico, Human Genetics Program, University Center for Health Sciences, Guadalajara, Mexico; Díaz-Rodriguez, M., Genetics Division, Biomedical Research Center, West-Mexican Social Security Institute, Guadalajara, Mexico, Human Genetics Program, University Center for Health Sciences, Guadalajara, Mexico; Nastasi-Catanese, J.A., Genetics Division, Biomedical Research Center, West-Mexican Social Security Institute, Guadalajara, Mexico, Human Genetics Program, University Center for Health Sciences, Guadalajara, Mexico, University of East Nucleus Bolivar, Genetics Unit, Ciudad Bolivar, Bolivar, Venezuela; Toscano-Flores, J.J., Genetics Division, Biomedical Research Center, West-Mexican Social Security Institute, Guadalajara, Mexico, Human Genetics Program, University Center for Health Sciences, Guadalajara, Mexico; Bañuelos-Robles, O., Radiological Studies Private Unit Drs. Bañuelos, Guadalajara, Mexico; Figuera, L.E., Genetics Division, Biomedical Research Center, West-Mexican Social Security Institute, Guadalajara, Mexico, Human Genetics Program, University Center for Health Sciences, Guadalajara, Mexico; Matute, E., Neurosciences Institute, University Center for Biological and Agricultural Sciences, University of Guadalajara, Guadalajara, Mexico; De Lourdes Ramirez-Duenas, M., Genetics Division, Biomedical Research Center, West-Mexican Social Security Institute, Guadalajara, Mexico, Human Genetics Program, University Center for Health Sciences, Guadalajara, Mexico, División de Genética, CIBO-IMSS, Sierra Mojada 800, C.P. 44340, Guadalajara, Jalisco, Mexico
dc.relation.isReferencedByScopus
dc.relation.isReferencedByWOS
dc.identifier.urlhttp://www.scopus.com/inward/record.url?eid=2-s2.0-41849123119&partnerID=40&md5=6d286360e652c7900ade2851f0da2f1d
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