Prenatal features of 17q12 microdeletion and microduplication syndromes: A retrospective case series
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference32 articles.
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1. Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - A retrospective cohort study and literature review;Heliyon;2024-09
2. Chromosomal abnormalities detected by chromosomal microarray analysis and pregnancy outcomes of 4211 fetuses with high-risk prenatal indications;Scientific Reports;2024-07-10
3. Concurrent of compound heterozygous variant of a novel in-frame deletion and the common hypomorphic haplotype in TBX6 and inherited 17q12 microdeletion in a fetus;BMC Pregnancy and Childbirth;2024-07-01
4. Prenatal Genetic Analysis of Fetal 17q12 Microdeletion Syndrome and Relation to Kidney Abnormalities;2023-05-25
5. Genetic autopsy and genetic counseling for a case of fatal oligohydramnios due to de novo 17q12 deletion syndrome;Journal of Obstetrics and Gynaecology Research;2023-03-12
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