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OC06.04: Population‐based prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort
Author(s) -
Hui L.,
Poulton A.,
Kluckow E.,
Lindquist A.,
Hutchinson B.,
Pertile M.D.,
Bonacquisto L.,
Gugasyan L.,
Kulkarni A.,
Harraway J.,
Howden A.,
McCoy R.,
da Silva Costa F.,
Menezes M.,
PalmaDias R.,
Nisbet D.,
Martin N.,
Bethune M.,
Poulakis Z.,
Halliday J.
Publication year - 2019
Publication title -
ultrasound in obstetrics and gynecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.202
H-Index - 141
eISSN - 1469-0705
pISSN - 0960-7692
DOI - 10.1002/uog.20459
Subject(s) - medicine , miscarriage , snp array , population , obstetrics , pregnancy , prenatal diagnosis , products of conception , chromosome , cohort , fetus , genetics , single nucleotide polymorphism , biology , gestation , pathology , genotype , gene , environmental health