Terminal deletion of the short arm of chromosome 3

dc.contributorLizcano-Gil, L.A., Division de Genetica, Ap Postal 1-3838, Guadalajara, Jalisco, Mexico; Figuera, L.E., Division de Genetica, Ap Postal 1-3838, Guadalajara, Jalisco, Mexico
dc.creatorLizcano-Gil, L.A.
dc.creatorFiguera, L.E.
dc.date.accessioned2015-11-19T18:57:47Z
dc.date.accessioned2023-07-03T23:02:27Z
dc.date.available2015-11-19T18:57:47Z
dc.date.available2023-07-03T23:02:27Z
dc.date.created2015-11-19T18:57:47Z
dc.date.issued1994
dc.identifierhttp://hdl.handle.net/20.500.12104/71205
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0028220413&partnerID=40&md5=42c10b84cc7a2b4f53cce660c89e59d7
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/7247926
dc.description.abstractDeletion of the short arm of chromosome number 3, has been proposed as a distinctive syndrome, all cases are (de novo) deletions and the band 3p26 was systematically involved. The comparative study of the 21 reviewed cases (including one reported here) allows to conclude that there is no consistent association to delineate a typical clinical syndrome.
dc.relationGenetic Counseling
dc.relation5
dc.relation1
dc.relation35
dc.relation38
dc.relationScopus
dc.titleTerminal deletion of the short arm of chromosome 3
dc.typeArticle


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