High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2

Genes Chromosomes and Cancer

Volumn 18, Issue 1, 1997, Pages 50-58

  Scheurlen, Wolfram G ^a   Seranski, Peter ^b   Mincheva, Antonia ^b   Kühl, Joachim ^a   Sörensen, Niels ^a   Krauss, Jürgen ^a   Lichter, Peter ^b   Poustka, Annemarie ^b   Wilgenbus, Klaus K ^b  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 17P; CHROMOSOME ABERRATION; CHROMOSOME MAP; CYTOGENETICS; GENE DELETION; GENE DISRUPTION; GENETIC HETEROGENEITY; HUMAN; HUMAN TISSUE; KARYOTYPING; MALIGNANT TRANSFORMATION; NEUROECTODERM TUMOR; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; STEM CELL;

ADOLESCENT; ADULT; BRAIN NEOPLASMS; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; DNA, NEOPLASM; FEMALE; GENE DELETION; GENES, TUMOR SUPPRESSOR; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INTERPHASE; MALE; METAPHASE; MICROSATELLITE REPEATS; NEUROECTODERMAL TUMORS; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;

EID: 0031014667     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199701)18:1<50::AID-GCC6>3.0.CO;2-0     Document Type: Article

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