Please use this identifier to cite or link to this item: http://sgc.anlis.gob.ar/handle/123456789/611
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dc.contributor.authorZeiger, Joanna Sen_US
dc.contributor.authorHetmanski, Jacqueline Ben_US
dc.contributor.authorBeaty, Terri Hen_US
dc.contributor.authorVanderKolk, Craig Aen_US
dc.contributor.authorWyszynski, Diego F.en_US
dc.contributor.authorBailey-Wilson, Joan Een_US
dc.contributor.authorde Luna, Rosa Ortizen_US
dc.contributor.authorPerandones, Claudiaen_US
dc.contributor.authorTolarova, Marie Men_US
dc.contributor.authorMosby, Terezieen_US
dc.contributor.authorBennun, Ricardo D.en_US
dc.contributor.authorSegovia, Mabelen_US
dc.contributor.authorCalda, Pavelen_US
dc.contributor.authorPugh, Elizabeth Wen_US
dc.contributor.authorDoheny, Kimen_US
dc.contributor.authorMcIntosh, Iainen_US
dc.date.accessioned2019-05-15T04:18:11Z-
dc.date.available2019-05-15T04:18:11Z-
dc.date.issued2003-11-
dc.identifier.issn1018-4813-
dc.identifier.urihttps://doi.org/10.1038/sj.ejhg.5201052-
dc.identifier.urihttp://sgc.anlis.gob.ar/handle/123456789/611-
dc.description.abstractResults from a genome-wide screen of 10 multiplex families ascertained through probands with nonsyndromic cleft lip with or without cleft palate (CL/P) in Mexico, Argentina, and the United States yielded suggestive evidence of linkage to chromosomes 2, 6, 17 and 18. Fine mapping excluded all regions except chromosome 2. Subsequent analysis was performed on the original 10 families plus an additional 16 families using 31 markers on chromosome 2. This analysis showed intriguing evidence of linkage to 2q (Zlr=2.26, empirical P-value=0.028 in a chromosome-wide analysis). Transmission disequilibrium tests also revealed evidence of linkage and disequilibrium for two markers in this region (D2S168 and D2S1400 with P-values=0.022 and 0.006, respectively). A subset of these 26 families provided additional evidence for a susceptibility gene for CL/P on 2q, suggesting that further studies of genes in this region are warranted.en_US
dc.language.isoenen_US
dc.relation.ispartofEuropean journal of human genetics : EJHGen_US
dc.subjectMapeo Cromosómicoen_US
dc.subjectFisura del Paladaren_US
dc.subjectLabio Leporinoen_US
dc.subjectLigamiento Genéticoen_US
dc.subjectMarcadores Genéticosen_US
dc.subjectPredisposición Genética a la Enfermedaden_US
dc.subjectPruebas Genéticasen_US
dc.titleEvidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2en_US
dc.typeArtículoen_US
dc.identifier.doi10.1038/sj.ejhg.5201052-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeArtículo-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.deptUnidad Ejecutora de Formación y Educación Superior (UEFES)-
crisitem.author.deptCentro Nacional de Genética Médica (CeNaGeM)-
crisitem.author.parentorgAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.parentorgAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
Appears in Collections:Publicaciones CeNaGeM
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