Microarrays in prenatal diagnosis
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology,General Medicine
Reference102 articles.
1. Genomic microarrays: a technology overview;Brady;Prenat Diagn,2012
2. Chromosome microarrays in human reproduction;Rajcan-Separovic;Hum Reprod Update,2012
3. Whole-genome array as a first-line cytogenetic test in prenatal diagnosis;Srebniak;Ultrasound Obstet Gynecol,2015
4. Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotyping;Bruno;J Med Genet,2011
5. Diagnostic implications of excessive homozygosity detected by SNP-based microarrays: consanguinity, uniparental disomy, and recessive single-gene mutations;Kearney;Clin Lab Med,2011
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1. The Impact of Chromosomal Mosaicisms on Prenatal Diagnosis and Genetic Counseling—A Narrative Review;Journal of Personalized Medicine;2024-07-21
2. Prenatal Chromosomal Microarray Analysis: Does Increased Resolution Equal Increased Yield?;Genes;2023-07-25
3. Prenatal Diagnosis of Chromosomal Mosaicism in 18,369 Cases of Amniocentesis;American Journal of Perinatology;2023-06-19
4. Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China;Scientific Reports;2023-05-04
5. Validation and depth evaluation of low-pass genome sequencing in prenatal diagnosis using 387 amniotic fluid samples;Journal of Medical Genetics;2023-04-03
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