IDENTIFICATION BY FLUORESCENCE OF 2 G RINGS 46XY21R GDELETION SYNDROME I AND 46XX22R GDELETION SYNDROME II

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dc.contributor.authorWELEBER, RG
dc.contributor.authorOVERTON, K
dc.contributor.authorMAGENIS, RE
dc.contributor.authorHECHT, F
dc.contributor.authorARMENDARES, S
dc.date.accessioned2026-05-28T16:31:45Z
dc.date.issued1972
dc.description.paginacion265 - 266
dc.description.procedenciaEXT
dc.format.discursoNota
dc.format.extent2
dc.identifier.issn0003-3995
dc.identifier.urihttps://ahcm.cinvestav.mx/handle/ahcm/23339
dc.language.isoInglés
dc.numero.secuencia23336
dc.publisherUNIV OREGON,CHILD DEV & REHABIL CTR,MED SCH,DIV MED GENET,CYTOGENET LABS,PORTLAND,OR 97201
dc.publisherHOSP PEDIAT,CTR MED NACL,DEPT MED GENET,MEXICO CITY 7,MEXICO
dc.relation.ispartofseriesVol. 15 No. 4
dc.source.revistafuenteANNALES DE GENETIQUE
dc.subjectIDENTIFICATION, FLUORESCENCE, 2 G RINGS 46,XY,21R , G DELETION I, SYNDROME 46,XX,22R , G DELETION SYNDROME II
dc.subject.categoriaprincipalCIENCIAS DE LA VIDA
dc.subject.disciplinaBIOLOGIA HUMANA
dc.subject.subdisciplinaGENETICA HUMANA
dc.titleIDENTIFICATION BY FLUORESCENCE OF 2 G RINGS 46XY21R GDELETION SYNDROME I AND 46XX22R GDELETION SYNDROME II
dc.title.alternativeANN GENET PARIS

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