Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium

Cytogenetics and Cell Genetics

Volumn 91, Issue 1-4, 2000, Pages 141-147

  Kutsche, K ^a   Glauner, E ^a   Knauf, S ^a   Pomarino, A ^a   Schmidt, M ^a   Schroder B ^a   Nothwang, H G ^b   Schuler H M ^c   Goecke, T O ^c   Kersten, A J ^d   Althaus, C ^d   Gal, A ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^c HEINRICH HEINE UNIVERSITY   (Germany)

^d UNIVERSITY HOSPITAL DÜSSELDORF   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 11P; CHROMOSOME 18P; CHROMOSOME TRANSLOCATION 11; CHROMOSOME TRANSLOCATION 18; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MUTATION; HAMARTOMA; HUMAN; MALE; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; PIGMENT EPITHELIUM; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

EID: 0034490183     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: 10.1159/000056835     Document Type: Article

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