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Original Communication - Genomic and expression array profiling of chromosome 20q amplicon in human colon cancer cells, 12/2005
Background: Gain of the q arm of chromosome 20 in human colorectal cancer has been associated with poorer survival time and has been reported to increase in... 
Cancer, Array-CGH, Amplification, Genomic Profiling
Journal
NATURE REVIEWS GENETICS, ISSN 1471-0056, 05/2011, Volume 12, Issue 5, pp. 363 - 375
Comparisons of human genomes show that more base pairs are altered as a result of structural variation - including copy number variation - than as a result of... 
COMBINATORIAL ALGORITHMS | VARIANTS | DNA | GENETICS & HEREDITY | RECENT SEGMENTAL DUPLICATIONS | FINE-SCALE | ACCURATE DETECTION | POLYMORPHISM | RESOLUTION ARRAY CGH | COPY-NUMBER VARIATION | REAL-TIME
Journal Article
Seizure: European Journal of Epilepsy, ISSN 1059-1311, 04/2018, Volume 57, pp. 63 - 65
We report a de novo 12q22–q23.3 duplication detected by whole-genome array comparative genomic hybridization (array-CGH) in a 5-year-old girl with temporal... 
Array-CGH | Temporal lobe epilepsy | 12q22q23.3
Journal Article
Genetics and molecular biology, ISSN 1415-4757, 08/2019
Duplication of the short arm of chromosome 12 is a rare chromosomal abnormality that may arise de novo or result from malsegregation of a balanced parental... 
duplication 12p | array-CGH | facial dysmorphism
Journal Article
Reproductive BioMedicine Online, ISSN 1472-6483, 08/2019, Volume 39, pp. e54 - e54
Journal Article
Molecular Cell, ISSN 1097-2765, 05/2015, Volume 58, Issue 4, pp. 598 - 609
Journal Article
Oncogene, ISSN 0950-9232, 03/2016, Volume 35, Issue 10, pp. 1216 - 1224
Journal Article
Nature Reviews Genetics, ISSN 1471-0056, 05/2018, Volume 19, Issue 5, pp. 253 - 268
The majority of rare diseases affect children, most of whom have an underlying genetic cause for their condition. However, making a molecular diagnosis with... 
ONSET CONDITIONS | INCIDENTAL FINDINGS | COST-EFFECTIVENESS | ONLINE MENDELIAN INHERITANCE | ARRAY-CGH | GENETICS & HEREDITY | AMERICAN-COLLEGE | MEDICAL GENETICS | VARIANT | GENETIC RISK SCORE | CLINICAL EXOME | Disease | Genomics | Genetic diversity | Children | Diagnosis | Medical diagnosis | Population genetics
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 04/2009, Volume 84, Issue 4, pp. 524 - 533
Journal Article
Nature, ISSN 0028-0836, 11/2006, Volume 444, Issue 7118, pp. 444 - 454
Journal Article