Prenatal Diagnosis of Trisomy 13
Author:
Publisher
Wiley
Subject
Radiology Nuclear Medicine and imaging,Radiological and Ultrasound Technology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.7863/jum.2006.25.4.429/fullpdf
Reference26 articles.
1. The pathology of trisomy 13 syndrome
2. A common ancestral haplotype in carrier chromosomes from different ethnic backgrounds in vacuolating megalencephalic leucoencephalopathy with subcortical cysts
3. Maternal Age and Gestational Age-Specific Risk for Chromosomal Defects
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1. Trisomy 18, Trisomy 13, and Other Aneuploidies;Down Syndrome Screening;2023
2. Rapid confirmation of trisomy 13 of maternal origin by QF-PCR following postmortem tissue cell culture failure in a pregnancy with trisomy 13 at amniocentesis and fetal postaxial polydactyly and facial cleft;Taiwanese Journal of Obstetrics and Gynecology;2022-11
3. Application of quantitative fluorescent polymerase chain reaction analysis for the rapid confirmation of trisomy 13 of maternal origin in a pregnancy with fetal holoprosencephaly, cyclopia, polydactyly, omphalocele and cell culture failure;Taiwanese Journal of Obstetrics and Gynecology;2022-01
4. Rapid diagnosis of trisomy 13 of maternal origin by quantitative fluorescent polymerase chain reaction analysis in a pregnancy with fetal holoprosencephaly, premaxillary agenesis, postaxial polydactyly of left hand and overriding aorta;Taiwanese Journal of Obstetrics and Gynecology;2021-09
5. First-trimester presentation of ultrasound findings in trisomy 13 and validation of multiparameter ultrasound-based risk calculation models to detect trisomy 13 in the late first trimester;Journal of Perinatal Medicine;2020-10-19
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