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Retinoblastoma in a patient with a 13qXp translocation.

Abstract：

:An infant girl with failure to thrive and bilateral retinoblastoma had a translocation of the long arm of chromosome 13 to the short arm of the X chromosome, and possible loss of a portion of the q 14 band. The lack of other major organ malformations in this patient emphasized the importance of considering chromosomal aberrations as a possible etiology of retinoblastoma in patients with nonspecific psychomotor retardation.

journal_name

Am J Ophthalmol

journal_title

American journal of ophthalmology

authors

Cross HE,Hansen RC,Morrow G 3rd,Davis JR

doi

10.1016/0002-9394(77)90450-0

subject

Has Abstract

pub_date

1977-10-01 00:00:00

pages

548-54

issue

4

eissn

0002-9394

issn

1879-1891

pii

0002-9394(77)90450-0

journal_volume

84

pub_type

杂志文章

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