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PMID: 6521998 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't

Incidence and significance of a deletion of chromosome band 13q14 in patients with retinoblastoma and in their families.

Ophthalmology ·Vol. 91 ·No. 12 ·1984-12-00 ·Pages 1695-9

Liberfarb RM, Bustos T, Miller WA, Sang D

Abstract

Ten unrelated retinoblastoma patients were studied cytogenetically with high-resolution prophase banding; two had a deletion of chromosome 13, band q14. Neither of the two patients had any of the congenital defects usually associated with 13q14 deletions. In patient A, the deletion was found to be de novo. Patient B was found to be mosaic for the 13q14 deletion with 54% of the lymphocytes examined having the deletion. This study indicates that the 13q14 deletion may occur in a significant portion of all retinoblastoma cases. Esterase D activity and isozymes were studied also. The significance of findings will be discussed.

MeSH Terms
Carboxylesterase Carboxylic Ester Hydrolases/genetics Child, Preschool Chromosome Banding Chromosome Deletion Chromosomes, Human, 13-15 Eye Neoplasms/enzymology,genetics Female Genetic Counseling Humans Infant Isoenzymes/genetics Male Mosaicism Retinoblastoma/enzymology,genetics
Chemicals
Isoenzymes Carboxylic Ester Hydrolases Carboxylesterase ESD protein, human
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Liberfarb R M
Bustos T
Miller W A
Sang D
Article Info
Journal
Ophthalmology
Abbr.
Ophthalmology
ISSN
0161-6420
Published
1984-12-00
Pages
1695-9
Language
English
Region
United States
NLM ID
7802443
Subset
IM
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