Description:
RETINOBLASTOMA, SPORADIC
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Heritable Diseases dbGaP |
Class |
Ophthalmologic Disorders |
Quantity |
25 µg |
Quantitation Method |
Please see our FAQ |
Biopsy Source
|
Peripheral vein
|
Cell Type
|
B-Lymphocyte
|
Tissue Type
|
Blood
|
Transformant
|
Epstein-Barr Virus
|
Sample Source
|
DNA from LCL
|
Race
|
White
|
Family Member
|
1
|
Relation to Proband
|
proband
|
Confirmation
|
Clinical summary/Case history
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase Isoenzyme Electrophoresis and by Chromosome Analysis |
|
Cytogenetics |
Chromosome 13: DELETION Aneuploid Segment (-)13q14>13q22 |
Remarks |
Bilateral; 46,XX,del(13)(pter>q14.1:: q22.1>qter) in fibroblasts; see GM01142A Fibroblast and GM03022 SV40 Transformed Fibroblast |
Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP, A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds G3 (Bethesda, Md)3:1143-9 2013 |
PubMed ID: 23665875 |
|
Wang L, Rao M, Fang Y, Hameed M, Viale A, Busam K, Jhanwar SC., A Genome-Wide High-Resolution Array-CGH Analysis of Cutaneous Melanoma and Comparison of Array-CGH to FISH in Diagnostic Evaluation. J Mol Diagn.15(5):581-91 2013 |
PubMed ID: 23800576 |
|
Barr FG, Sellinger B, Emanuel BS, Localization of the rhabdomyosarcoma t(2;13) breakpoint on a physical map of chromosome 13. Genomics11:941-7 1991 |
PubMed ID: 1783402 |
|
Higgins MJ, Turmel C, Noolandi J, Neumann PE, Lalande M, Construction of the physical map for three loci in chromosome band 13q14: comparison to the genetic map. Proc Natl Acad Sci U S A87:3415-9 1990 |
PubMed ID: 1970636 |
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