Wanjun Wang
Nanjing University
10 Papers
15 Citations
Wanjun Wang is an academic researcher from Nanjing University. The author has contributed to research in topics: Prenatal diagnosis & Medicine. The author has an hindex of 3, co-authored 7 publications.
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Papers
Application of chromosomal microarray analysis in products of miscarriage.
TL;DR: Chromosomal microarray testing should be referred to couples at their first miscarriage regardless of the way how they get pregnant, because of the potential impact on previous guidelines and the present management on miscarried couples and products.
The application of chromosomal microarray analysis to the prenatal diagnosis of isolated mild ventriculomegaly.
TL;DR: It is suggested that CNVs could aid in the risk assessment and genetic counseling in fetuses with isolated mild ventriculomegaly in a manner similar to conventional karyotyping.
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Long-read sequencing: An effective method for genetic analysis of CYP21A2 variation in congenital adrenal hyperplasia.
TL;DR: In this paper , the authors evaluated the clinical utility of the long read sequencing (LRS) method in carrier screening and genetic diagnosis of congenital adrenal hyperplasia (CAH) by comparing the efficiency of the LRS method with the conventional multiplex ligation-dependent probe amplification (MLPA) plus Sanger sequencing approaches in CYP21A2 analysis.
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A boy with partial trisomy of chromosome 3q24–q28 from paternal balanced insertion and multiple congenital anomalies
TL;DR: The genotype and phenotype of a 32‐month‐old boy with a partial trisomy of 3q24–q28 is described, which included severe mental retardation, postnatal developmental delay, ventricular septal defect (VSD), and craniofacial anomalies including cleft palate, frontal bossing, hypertelorism, and a broad nasal bridge.
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[Prenatal diagnosis and follow-up of a case with Lowe syndrome caused by interstitial deletion of Xq25-26]
TL;DR: Prenatal diagnosis of Lowe syndrome without a family history largely depends on fetal imaging, and should cataract be found by ultrasound screening, fetal MRI may be considered to rule out central nervous system anomalies.
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