Complex Chromosome Rearrangement (CCR) involving chromosomes 2, 5, 11, and 16 and a reciprocal translocation between chromosomes 6 and 8 verified by spectral karyotyping (SKY) in a girl with mild dysmorphic features and mental retardation.

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dc.contributor.authorRamos, E. S.
dc.contributor.authorRogatto, Silvia Regina [UNESP]
dc.contributor.authorMartelli, L.
dc.contributor.authorPiram, A.
dc.contributor.authorSantos, S. A.
dc.contributor.authorSquire, J. A.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionSinha Junqueira Matern Fdn
dc.contributor.institutionUniv Toronto
dc.date.accessioned2014-05-20T13:50:02Z
dc.date.available2014-05-20T13:50:02Z
dc.date.issued1999-10-01
dc.description.affiliationUniv São Paulo, Sch Med Ribeirao Preto, Dept Genet, Ribeirao Preto, SP, Brazil
dc.description.affiliationUNESP, Inst Biociencias, Dept Genet, Botucatu, SP, Brazil
dc.description.affiliationSinha Junqueira Matern Fdn, Div Genet, Ribeirao Preto, SP, Brazil
dc.description.affiliationUniv Toronto, Princess Margaret Hosp, Ontario Canc Inst, Toronto, ON, Canada
dc.description.affiliationUnespUNESP, Inst Biociencias, Dept Genet, Botucatu, SP, Brazil
dc.format.extentA356-A356
dc.identifierhttp://www.academia.edu/3490307/ICSI-gestational_Carrier_Association_as_a_Strategy_for_Treatment_of_Mayer-_Rokitansky-Kuster-Hauser_Syndrome_Patients_Case_Report_and_Literature_Review
dc.identifier.citationAmerican Journal of Human Genetics. Chicago: Univ Chicago Press, v. 65, n. 4, p. A356-A356, 1999.
dc.identifier.issn0002-9297
dc.identifier.urihttp://hdl.handle.net/11449/17846
dc.identifier.wosWOS:000082879802013
dc.language.isoeng
dc.publisherUniv Chicago Press
dc.relation.ispartofAmerican Journal of Human Genetics
dc.relation.ispartofjcr8.855
dc.relation.ispartofsjr7,450
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.titleComplex Chromosome Rearrangement (CCR) involving chromosomes 2, 5, 11, and 16 and a reciprocal translocation between chromosomes 6 and 8 verified by spectral karyotyping (SKY) in a girl with mild dysmorphic features and mental retardation.en
dc.typeResumo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderUniv Chicago Press
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências, Botucatupt

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