Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities

American Journal of Human Genetics

Volumn 98, Issue 1, 2016, Pages 34-44

  Lo, Kitty K ^a   Karampetsou, Evangelia ^b   Boustred, Christopher ^b   McKay, Fiona ^b   Mason, Sarah ^b   Hill, Melissa ^b   Plagnol, Vincent ^a   Chitty, Lyn S ^b,c  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b GREAT ORMOND STREET HOSPITAL   (United Kingdom)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALGORITHM; ANEUPLOIDY; ARTICLE; CHROMOSOME 12; CHROMOSOME 18; CHROMOSOME ABERRATION; DIAGNOSTIC TEST; FEMALE; FETUS; GENE SEQUENCE; GENOME; HUMAN; MATERNAL PLASMA; NON INVASIVE PRENATAL TESTING; NON INVASIVE PROCEDURE; PATHOGENICITY; PRIORITY JOURNAL; SENSITIVITY ANALYSIS; STANDARD; SUBCHROMOSOMAL ABNORMALITY; GENETIC SCREENING; HIGH THROUGHPUT SEQUENCING; PREGNANCY; PRENATAL DIAGNOSIS; PROCEDURES; STANDARDS;

ANEUPLOIDY; CHROMOSOME ABERRATIONS; FEMALE; GENETIC TESTING; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 84954285965     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2015.11.016     Document Type: Article

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