Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases

Molecular Cytogenetics

Volumn 4, Issue 1, 2011, Pages

  Park, Sang Jin ^a   Jung, Eun Hye ^a   Ryu, Ran Suk ^a   Kang, Hyun Woong ^b   Ko, Jung Min ^c   Kim, Hyon J ^c   Cheon, Chong Kun ^d   Hwang, Sang Hyun ^e   Kang, Ho Young ^a  

^a MG MED Inc   (South Korea)

^b Macrogen Inc   (South Korea)

^c Ajou University School of Medicine   (South Korea)

^d Pusan National University School of Medicine   (South Korea)

^e National Cancer Center   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANEUPLOIDY; ARTICLE; CHORION VILLUS; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; COPY NUMBER VARIATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE; MAJOR CLINICAL STUDY; PERINATAL PERIOD; PHENOTYPE; PRENATAL PERIOD; PRIORITY JOURNAL; UMBILICAL CORD BLOOD;

EID: 79955683789     PISSN: None     EISSN: 17558166     Source Type: Journal    
DOI: 10.1186/1755-8166-4-12     Document Type: Article

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