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Unbalanced 5;16 translocation in a boy with papillary thyroid carcinoma
Author(s) -
McDonald M.,
Maynard S.,
Sheldon S.,
Innis J.
Publication year - 1994
Publication title -
american journal of medical genetics
Language(s) - English
Resource type - Journals
eISSN - 1096-8628
pISSN - 0148-7299
DOI - 10.1002/ajmg.1320490309
Subject(s) - chromosomal translocation , monosomy , thyroid carcinoma , trisomy , thyroid , papillary carcinoma , chromosome , etiology , pathology , karyotype , medicine , biology , genetics , gene
This is the first reported case of an unbalanced chromosome rearrangement resulting in trisomy 5q35.5 → qter and monosomy 16p 13.3 → pter, in a boy with mental and growth retardation, minor anomalies, and a history of bilateral papillary thyroid carcinoma. This was the result of a familial balanced translocation. The clinical and cytogenetic manifestations of the case are presented and the possible role of the chromosomal rearrangement in the etiology of the thyroid carcinoma is discussed. © 1994 Wiley‐Liss, Inc.

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