Array comparative genetic hybridisation in clinical diagnostics: Principles and applications

LaboratoriumsMedizin

Volumn 33, Issue 5, 2009, Pages 255-266

  Heinrich, Uwe ^a   Rost, Imma ^a   Brown, Anthony ^b   Gordon, Tony ^b   Haan, Nick ^b   Massie, Jessica ^b  

^a Laboratory Medicine Dr Klein and Dr Rost   (Germany)

^b ILLUMINA INC   (United States)

Author keywords

Array comparative genetic hybridisation (aCGH); Copy number variant (CMV); Mental retardation; Microdeletions; Microduplications; Prenatal diagnostics

Indexed keywords

ARTICLE; AUTISM; CANCER DIAGNOSIS; CHILD; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CONGENITAL MALFORMATION; DATA ANALYSIS; DEVELOPMENTAL DISORDER; DNA EXTRACTION; DNA HYBRIDIZATION; DNA SEQUENCE; HUMAN; MENTAL DEFICIENCY; PATIENT SELECTION; PRENATAL DIAGNOSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 70349311578     PISSN: 03423026     EISSN: 14390477     Source Type: Journal    
DOI: 10.1515/JLM.2009.045     Document Type: Article

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