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oai:serval.unil.ch:BIB_A12922FB3702
2024-03-23T02:46:10Z
serval:BIB_A12922FB3702
Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomalies
11262644
L.
Lavanchy
author
F. L.
Munier
author
P.
Cousin
author
A. C.
Gaide
author
F.
Thonney
author
D. F.
Schorderet
author
article
2001-03
Ophthalmic Genetics
1381-6810
journal
22
1
1-10
Child, Preschool
Chromosome Fragility
*Chromosome Mapping
*Chromosomes, Human, Pair 13
Clone Cells
DNA/analysis
Facies
Female
*Gene Deletion
Genetic Markers
Humans
Infant
Male
Retinal Neoplasms/*genetics/pathology
Retinoblastoma/*genetics/pathology
Syndrome
Journal Article --- Old month value: Mar
60_published