dc.contributorRivera, H., División De Genética, Instituto Mexicano del Seguro Social, Ap. Postal 1-3838, Guadalajara, Jalisco, Mexico, Doctorado En Genética Humana, Universidad De Guadalajara, Guadalajara, Jalisco, Mexico; Gutiérrez-Angulo, M., División De Genética, Instituto Mexicano del Seguro Social, Ap. Postal 1-3838, Guadalajara, Jalisco, Mexico, Doctorado En Genética Humana, Universidad De Guadalajara, Guadalajara, Jalisco, Mexico; Gómez-Sánchez, H., División De Genética, Instituto Mexicano del Seguro Social, Ap. Postal 1-3838, Guadalajara, Jalisco, Mexico; Macías-Gómez, N., División De Genética, Instituto Mexicano del Seguro Social, Ap. Postal 1-3838, Guadalajara, Jalisco, Mexico, Doctorado En Genética Humana, Universidad De Guadalajara, Guadalajara, Jalisco, Mexico; Barros-Núñez, P., División De Genética, Instituto Mexicano del Seguro Social, Ap. Postal 1-3838, Guadalajara, Jalisco, Mexico, Doctorado En Genética Humana, Universidad De Guadalajara, Guadalajara, Jalisco, Mexico
dc.creatorRivera, H.
dc.creatorGutierrez-Angulo, M.
dc.creatorGomez-Sanchez, H.
dc.creatorMacias-Gomez, N.
dc.creatorBarros-Nunez, P.
dc.date.accessioned2015-11-19T18:55:27Z
dc.date.accessioned2022-11-02T14:18:10Z
dc.date.available2015-11-19T18:55:27Z
dc.date.available2022-11-02T14:18:10Z
dc.date.created2015-11-19T18:55:27Z
dc.date.issued2002
dc.identifierhttp://hdl.handle.net/20.500.12104/68409
dc.identifier10.1016/S0003-3995(02)01112-7
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0036021291&partnerID=40&md5=66c0ef75b456b354e4cae110a88d2640
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4995196
dc.description.abstractA boy with Down syndrome due to a free trisomy 21 also had a metacentric Y chromosome with an arm euchromatic and the other heterochromatic inherited from his phenotypically normal father. This chromosome was mitotically stable and hybridized with the DYZ3 probe precisely at its primary constriction; in addition, a subtelomeric Xp/Yp probe gave the expected signal near the end of the euchromatic arm. So, the proband's karyotype was 47,X,inv(Y)(p11q11.2),+21. Given the high frequency of both chromosome anomalies, we regard its concurrence as a mere coincidence. This observation, along with previous reports, allows us to classify the apparent pericentric inversions of the Y chromosome into two types: "true" inversions characterized by an alphoid single centromere and mitotic stability, and "false" inversions in which a nonalphoid centromere has taken over the usual alphoid centromere; indeed, these chromosomes are dicentric and mitotically unstable. Finally, the inv(Y) polymorphism in man compares with that documented in other mammal species, in which the rearranged Y chromosome neither impairs the fertility nor has other phenotypical consequences. © 2002 Éditions scientifiques et médicales Elsevier SAS. All rights reserved.
dc.relationAnnales de Genetique
dc.relation45
dc.relation2
dc.relation63
dc.relation65
dc.relationScopus
dc.relationWOS
dc.titleTrue vs. false inv(Y)(p11q11.2): A familial instance concurrent with trisomy 21
dc.typeArticle


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