Erratum to Clinical outcome of subchromosomal events detected by whole-genome noninvasive prenatal testing, [Prenat Diagn, (2015), 35, 999-1004] doi 10.1002/pd.4640;Clinical outcome of subchromosomal events detected by whole-genome noninvasive prenatal testing

Prenatal Diagnosis

Volumn 35, Issue 10, 2015, Pages 999-1004

  Helgeson, J ^a   Wardrop, J ^a   Boomer, T ^a   Almasri, E ^a   Paxton, W B ^a   Saldivar, J S ^a   Dharajiya, N ^a   Monroe, T J ^b   Farkas, D H ^c,d   Grosu, D S ^a   Mccullough, R M ^a  

^a SEQUENOM INC   (United States)

^b Sequenom Laboratories   (United States)

^c Sequenom Laboratories   (United States)

^d MICHIGAN STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALGORITHM; ARTICLE; BLOOD SAMPLING; CHROMOSOME ABERRATION; COPY NUMBER VARIATION; FALSE NEGATIVE RESULT; FALSE POSITIVE RESULT; FEMALE; FOLLOW UP; GENE SEQUENCE; HIGH RISK PATIENT; HUMAN; MAJOR CLINICAL STUDY; PREDICTIVE VALUE; PREGNANT WOMAN; PRENATAL SCREENING; PRIORITY JOURNAL; SUBCHROMOSOMAL ABERRATION; TRISOMY; GENE DELETION; HUMAN GENOME; MATERNAL SERUM SCREENING TEST; PREGNANCY;

FEMALE; GENE DELETION; GENOME, HUMAN; HUMANS; MATERNAL SERUM SCREENING TESTS; PREGNANCY;

EID: 84943267089     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.4810     Document Type: Erratum

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