Application of chromosomal microarray analysis and trio whole-exome sequencing in first-trimester prenatal diagnosis for high-risk pregnancies. [PDF]
Zhang Q +7 more
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Prenatal Diagnosis and Genotype-Phenotype Correlation in 8q21.11 Microdeletion Syndrome: A Case Report. [PDF]
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Statistical analysis and interpretation of prenatal diagnostic imaging studies, part 2: Descriptive and inferential statistical methods [PDF]
Odibo, Anthony O, Tuuli, Methodius G
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Evaluating the safety and outcomes of third-trimester selective termination in dichorionic twin pregnancies with discordant anomalies-a standardized approach for counseling. [PDF]
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Clinical application of fetal Nuchal Translucency combined with noninvasive prenatal testing in screening chromosome abnormalities. [PDF]
Fu G, Hu S.
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Ovarian Ectopic Pregnancy at 41-Week Gestation Age: A Case Report. [PDF]
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Ultrasound combined with molecular genetics to diagnose hereditary Renpenning syndrome in early pregnancy: a case report. [PDF]
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Part III: Clinical Departments and Divisions --- Chapter 20: Division of Medical Genetics (pages 396-398) [PDF]
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Identifying Differentially Methylated Sites for Methylation-Sensitive qPCR-based NIPT of Trisomies 13 and 18. [PDF]
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Chorionic villus sampling in the first trimester of pregnancy has the potential to become a major tool in the prenatal diagnosis and therapy of genetic disorders. Villus samples can be used for cytogenetic and biochemical studies as well as DNA analysis.
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