Use of prenatal chromosomal microarray: Prospective cohort study and systematic review and meta-analysis

Ultrasound in Obstetrics and Gynecology

Volumn 41, Issue 6, 2013, Pages 610-620

  Hillman, S C ^a   McMullan, D J ^b   Hall, G ^b   Togneri, F S ^b   James, N ^b   Maher, E J ^c   Meller, C H ^b,d   Williams, D ^b   Wapner, R J ^e   Maher, E R ^a,b   Kilby, M D ^a,b  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^b BIRMINGHAM CHILDREN S HOSPITAL NHS FOUNDATION TRUST   (United Kingdom)

^c WESTERN GENERAL HOSPITAL   (United Kingdom)

^d HOSPITAL ITALIANO DE BUENOS AIRES   (Argentina)

^e NewYork Presbyterian Hospital   (United States)

Author keywords

abnormal ultrasound findings; chromosomal microarray; G band karyotyping; prenatal diagnosis

Indexed keywords

CHROMOSOME DISORDER; FEMALE; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPING; META ANALYSIS; METHODOLOGY; MICROARRAY ANALYSIS; PREGNANCY; PRENATAL DIAGNOSIS; PROSPECTIVE STUDY; REVIEW; CHROMOSOME DISORDERS; PROCEDURES;

CHROMOSOME DISORDERS; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MICROARRAY ANALYSIS; PREGNANCY; PRENATAL DIAGNOSIS; PROSPECTIVE STUDIES; ULTRASONOGRAPHY, PRENATAL;

EID: 84879099857     PISSN: 09607692     EISSN: 14690705     Source Type: Journal    
DOI: 10.1002/uog.12464     Document Type: Review

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