TY  - GEN
AU  - Rostasy,K
AU  - Fauth,C
AU  - Gautsch,K
AU  - Laimer,I
AU  - Krabichler,B
AU  - Wimmer,K
AU  - Frühmesser,A
AU  - Kotzot,D
AU  - Moshir,S
TI  - Modification of risk for cancer as a coincidental finding in DNA array investigation
SN  - 1399-0004
PY  - 2013///0827
KW  - Adolescent
KW  - Checkpoint Kinase 2
KW  - Chromosome Deletion
KW  - Chromosome Disorders
KW  - diagnosis
KW  - Chromosomes, Human, Pair 22
KW  - genetics
KW  - Female
KW  - Humans
KW  - Incidental Findings
KW  - Magnetic Resonance Imaging
KW  - Neurofibromin 2
KW  - Neuroma, Acoustic
KW  - Oligonucleotide Array Sequence Analysis
KW  - methods
KW  - Protein Serine-Threonine Kinases
KW  - Risk Factors
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1399-0004.2012.01881.x
ER  -