Spectral Karyotyping for identification of constitutional chromosomal abnormalities at a national reference laboratory

Molecular Cytogenetics

Volumn 5, Issue 1, 2012, Pages

  Anguiano, Arturo ^a   Wang, Boris T ^a   Wang, Shirong R ^a   Boyar, Fatih Z ^a   Mahon, Loretta W ^a   El Naggar, Mohamed M ^a   Kohn, Peter H ^a   Haddadin, Mary H ^a   Sulcova, Vladimira ^a   Sbeiti, Adam H ^a   Ayad, Mervat S ^a   White, Beverly J ^a   Strom, Charles M ^a  

^a QUEST DIAGNOSTICS NICHOLS INSTITUTE   (United States)

Author keywords

array CGH; FISH; Marker Chromosome; Spectral Karyotyping

Indexed keywords

AMNIOCENTESIS; ARTICLE; CHROMOSOME; CHROMOSOME 15; CHROMOSOME 16; CHROMOSOME 2; CHROMOSOME ABERRATION; CHROMOSOME G BAND; CLINICAL LABORATORY; COMPARATIVE GENOMIC HYBRIDIZATION; COMPUTER PROGRAM; CONGENITAL MALFORMATION; CYTOGENETICS; DEVELOPMENTAL DISORDER; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPING; MAJOR CLINICAL STUDY; MARKER CHROMOSOME; MOSAICISM; MULTIPLE MALFORMATION SYNDROME; PERINATAL PERIOD; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SPECTRAL KARYOTYPING; SUPERNUMERARY CHROMOSOME;

EID: 84862778075     PISSN: None     EISSN: 17558166     Source Type: Journal    
DOI: 10.1186/1755-8166-5-3     Document Type: Article

References (19)

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