Case Reports
[VNTR-PCR in diagnosis of inherited Rb gene mutation]
[Article in
Polish]
Affiliations
- PMID: 7897998
Item in Clipboard
Case Reports
[VNTR-PCR in diagnosis of inherited Rb gene mutation]
[Article in
Polish]
Klin Oczna.
1994 Aug-Sep.
Abstract
Molecular genetic analysis of DNA by PCR-VNTR was performed in a family with hereditary retinoblastoma presenting some difficulties in pedigree analysis. PCR-VNTR allowed to perform a more accurate counselling in this family. Analysis of the way of transmission, carrier status exclusion (in two persons) and confirmation (in one) was possible only by VNTR-PCR.
Similar articles
-
[Genetics of retinoblastoma].Nihon Rinsho. 1995 Nov;53(11):2774-8. Nihon Rinsho. 1995. PMID: 8538043 Review. Japanese.
-
[Diagnosis of a predisposition of retinoblastoma at the DNA level].Gan To Kagaku Ryoho. 1991 Jan;18(1):44-50. Gan To Kagaku Ryoho. 1991. PMID: 1670986 Review. Japanese.
-
[RFLP-PCR technique for exclusion of carrier status of the mutated Rb gene].Klin Oczna. 1993 Jun;95(6):216-8. Klin Oczna. 1993. PMID: 7905940 Polish.
-
Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counseling.Klin Monbl Augenheilkd. 1996 May;208(5):400-3. doi: 10.1055/s-2008-1035252. Klin Monbl Augenheilkd. 1996. PMID: 8766064
-
[Prediction of retinoblastoma: linkage analysis of families with hereditary retinoblastoma by using polymorphic sites within the Rb gene].Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1995 Oct;17(5):338-42. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1995. PMID: 8706167 Chinese.
Publication types
MeSH terms
LinkOut - more resources
Other Literature Sources
Medical