Genetic assessment following increased nuchal translucency and normal karyotype
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.2718/fullpdf
Reference21 articles.
1. Increased nuchal translucency in euploid fetuses-what should we be telling the parents?;Bilardo;Prenat Diagn,2010
2. ACOG committee opinion no 432: spinal muscle atrophy;Committee on Genetics;Obstet Gynecol,2009
3. Prospective study of 22q11 deletion analysis in fetuses with excess nuchal translucency;Donnenfeld;Am J Obstet Gynecol,2006
4. A novel, single nucleotide polymorphism-based assay to detect 22q11 deletions;Fuenke;Genet Test,2007
5. Significance of chromosome 22q11 analysis after detection of an increased first-trimester nuchal translucency;Hollis;Ultrasound Obstet Gynecol,2001
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1. The Impact of Isolated Increased Nuchal Translucency ≥95th Centile on Perinatal Outcome: A Prospective Cohort Study from a North Indian Genetic Center;Journal of Fetal Medicine;2023-04
2. Diagnostic yield of copy number variation sequencing in fetuses with increased nuchal translucency: a retrospective study;Archives of Gynecology and Obstetrics;2023-01-05
3. Pregnancy outcomes of normal karyotype fetuses with increased nuchal translucency;CASP J INTERN MED;2023
4. Prenatal diagnosis of euploid increased nuchal translucency on fetal ultrasound (II): RASopathy disorders – Prenatal ultrasound findings and genotype–phenotype correlations;Journal of Medical Ultrasound;2023
5. Diagnostic yield of copy number variation sequencing in fetuses with increased nuchal translucency: A retrospective study;2022-10-27
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