| Literature DB >> 3587887 |
K Fujiki, Y Kuwabara, A Nakajima, I Nishigaki, T Ikeuchi.
Abstract
Esterase D was qualitatively and quantitatively analyzed in the red blood cells from 50 retinoblastoma patients who had been followed-up at Juntendo University and their family. In only one case with deletion of chromosome No. 13 (q12.3-q21.2), was the esterase D activity (type 2) 1.47 Unit/gHb which was approximately 50% of the level in normals. Additional retinoblastoma patients and their family members, 77 parents and 25 siblings, showed a normal range of esterase D level in their own phenotypes. These facts confirmed that the deletion of an esterase D locus was infrequent (approximately 2% in our series) in retinoblastoma patients. It was also compatible with the published data that the range of deletion of chromosome was No. 13 (q12.3-q21.2) involving 13q14.Entities:
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Year: 1987 PMID: 3587887 DOI: 10.3109/13816818709028510
Source DB: PubMed Journal: Ophthalmic Paediatr Genet ISSN: 0167-6784