Secondary findings from non-invasive prenatal testing for common fetal aneuploidies by whole genome sequencing as a clinical service

Prenatal Diagnosis

Volumn 33, Issue 6, 2013, Pages 602-608

  Lau, Tze Kin ^a   Jiang, Fu Man ^b   Stevenson, Robert J ^c   Lo, Tsz Kin ^d   Chan, Lin Wai ^e   Chan, Mei Ki ^b   Lo, Pui Shan Salome ^a   Wang, Wei ^b   Zhang, Hong Yun ^b   Chen, Fang ^b   Choy, Kwong Wai ^f,g  

^a Fetal Medicine Centre   (Hong Kong)

^b BGI SHENZHEN   (China)

^c Hong Kong Adventist Hospital   (Hong Kong)

^d KWONG WAH HOSPITAL   (Hong Kong)

^e UNITED CHRISTIAN HOSPITAL   (Hong Kong)

^f CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

^g CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMNIOCENTESIS; AMNION CELL; ANEUPLOIDY; ARTICLE; CHROMOSOME 18P; CHROMOSOME 21; CHROMOSOME 3; CHROMOSOME 7; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME MOSAICISM; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; FERTILIZATION IN VITRO; FETUS; FETUS MALFORMATION; GENE SEQUENCE; HUMAN; ISOCHROMOSOME; KARYOTYPE; KARYOTYPING; MOSAICISM; NON INVASIVE PRENATAL TESTING; PRENATAL SCREENING; PRIORITY JOURNAL; TETRASOMY; TRISOMY 18; TRISOMY 21; X CHROMOSOME;

ADULT; ANEUPLOIDY; CHROMOSOMES, HUMAN, PAIR 18; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, X; CLINICAL LABORATORY SERVICES; DNA; DOWN SYNDROME; FALSE NEGATIVE REACTIONS; FEMALE; FETUS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; PREGNANCY; PRENATAL DIAGNOSIS; TRISOMY;

EID: 84878129532     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.4076     Document Type: Article

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