Is high fetal nuchal translucency associated with submicroscopic chromosomal abnormalities on array CGH?

Ultrasound in Obstetrics and Gynecology

Volumn 43, Issue 6, 2014, Pages 620-624

  Huang, J ^a   Poon, L C ^b   Akolekar, R ^b,c   Choy, K W ^a,d   Leung, T Y ^a,d   Nicolaides, K H ^b  

^a CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

^b KING S COLLEGE HOSPITAL   (United Kingdom)

^c MEDWAY MARITIME HOSPITAL   (United Kingdom)

^d CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

array CGH; nuchal translucency; pathogenic submicroscopic CNV; prenatal array; prenatal diagnosis

Indexed keywords

ADULT; CHORION VILLUS SAMPLING; CHROMOSOME ABERRATION; COMPARATIVE GENOMIC HYBRIDIZATION; CROWN RUMP LENGTH; FEMALE; GESTATIONAL AGE; HUMAN; KARYOTYPE; NUCHAL TRANSLUCENCY MEASUREMENT; PREGNANCY; PREGNANCY OUTCOME; PROCEDURES;

ADULT; CHORIONIC VILLI SAMPLING; CHROMOSOME ABERRATIONS; COMPARATIVE GENOMIC HYBRIDIZATION; CROWN-RUMP LENGTH; FEMALE; GESTATIONAL AGE; HUMANS; KARYOTYPE; NUCHAL TRANSLUCENCY MEASUREMENT; PREGNANCY; PREGNANCY OUTCOME;

EID: 84901914228     PISSN: 09607692     EISSN: 14690705     Source Type: Journal    
DOI: 10.1002/uog.13384     Document Type: Article

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