Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12104/65007
Full metadata record
DC FieldValueLanguage
dc.contributor.authorCorona-Rivera, J.R.
dc.contributor.authorLopez-Marure, E.
dc.contributor.authorGarcia-Cruz, D.
dc.contributor.authorRomo-Huerta, C.O.
dc.contributor.authorRea-Rosas, A.
dc.contributor.authorOrozco-Alatorre, L.G.
dc.contributor.authorRamirez-Valdivia, J.M.
dc.date.accessioned2015-11-19T18:49:58Z-
dc.date.available2015-11-19T18:49:58Z-
dc.date.issued2009
dc.identifier.urihttp://hdl.handle.net/20.500.12104/65007-
dc.description.abstract[No abstract available]
dc.titleFurther clinical delineation of fine-lubinsky syndrome
dc.typeLetter
dc.identifier.doi10.1002/ajmg.a.32780
dc.relation.ispartofjournalAmerican Journal of Medical Genetics, Part A
dc.relation.ispartofvolume149
dc.relation.ispartofissue5
dc.relation.ispartofpage1070
dc.relation.ispartofpage1075
dc.contributor.affiliationCorona-Rivera, J.R., Instituto de Genetica Humana Dr. Enrique Corona-Rivera, Departamento de Biologia Molecular y Genomica, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico, Servicio de Genetica, Division de Pediatria, Hospital-Escuela, Guadalajara, Jalisco, Mexico, Clinica de Asesoramiento Genetico, Instituto de Genetica Humana Dr. Enrique Corona-Rivera, Centro Universitario de Ciencias de la Universidad de Guadalajara, Sierra Mojada 950, 44340 Guadalajara, Jalisco, Mexico; Lopez-Marure, E., Servicio de Radiologia, Division de Pediatria, Hospital-Escuela, Guadalajara, Jalisco, Mexico; Garcia-Cruz, D., Instituto de Genetica Humana Dr. Enrique Corona-Rivera, Departamento de Biologia Molecular y Genomica, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico; Romo-Huerta, C.O., Servicio de Oftalmologia, Division de Pediatria, Hospital-Escuela, Guadalajara, Jalisco, Mexico; Rea-Rosas, A., Servicio de Neurologia, Division de Pediatria, Hospital-Escuela, Guadalajara, Jalisco, Mexico; Orozco-Alatorre, L.G., Servicio de Genetica, Division de Pediatria, Hospital-Escuela, Guadalajara, Jalisco, Mexico; Ramirez-Valdivia, J.M., Servicio de Genetica, Division de Pediatria, Hospital-Escuela, Guadalajara, Jalisco, Mexico
dc.subject.headingIndex Medicus;Agenesis of Corpus Callosum;Cerebral Aqueduct/ab [Abnormalities];Craniosynostoses/di [Diagnosis];Craniosynostoses/ge [Genetics];Craniosynostoses/ra [Radiography];Developmental Disabilities/di [Diagnosis];Developmental Disabilities/ge [Genetics];Fingers/ab [Abnormalities];Humans;Hydrocephalus/di [Diagnosis];Hydrocephalus/ge [Genetics];Hydrocephalus/ra [Radiography];Infant;Magnetic Resonance Imaging;Male;Syndrome;Thorax/ab [Abnormalities]
dc.relation.isReferencedByScopus
dc.relation.isReferencedByMEDLINE
dc.relation.isReferencedByWOS
dc.identifier.urlhttp://www.scopus.com/inward/record.url?eid=2-s2.0-66849099870&partnerID=40&md5=8d1b2ee5831eeac927c4ec3e370f5a85
dc.identifier.urlhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&D=med5&AN=19396831
Appears in Collections:Producción científica UdeG (prueba)

Files in This Item:
There are no files associated with this item.


Items in RIUdeG are protected by copyright, with all rights reserved, unless otherwise indicated.