ExLibris header image
SFX Logo
Title: De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma
Source:

Human Genetics [0340-6717] Calzolari, E yr:1987


Collapse list of basic services Basic
Full text
Full text available via SpringerLINK Contemporary 1997-Present
GO
Full text available via SpringerLink Historical Archives Biomedical and Life Sciences
GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. Blanquet, V. "De novo t(2;13)(p24.3;q14.2) and retinoblastoma. Mapping of two 13q14 probes by in situ hybridization." Human genetics (1987): 102-105. Link to Full Text for this item Link to SFX for this item
2. Lalande, M. "Molecular detection and differentiation of deletions in band 13q14 in human retinoblastoma." Cancer genetics and cytogenetics 23.2: 151-157. Link to SFX for this item
3. Squire, J. "A detailed analysis of chromosomal changes in heritable and non-heritable retinoblastoma." Human genetics 70.4 (1985): 291-301. Link to Full Text for this item Link to SFX for this item
Select All Clear All

Expand list of advanced services Advanced
A service provided by the Library of the Wissenschaftspark Albert Einstein, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.