Central nervous system anomalies associated with fetal trisomy 18
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference3 articles.
1. (eds). 2000. Fetology, McGraw-Hill: New York; 997-1006.
2. Sex ratios in fetuses and liveborn infants with autosomal aneuploidy
3. Classifying sex biased congenital anomalies
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Comprehensive phenotyping of fetuses with trisomy 18: a perinatal center experience;Clinical Dysmorphology;2023-11-29
2. Rapid diagnosis of trisomy 18 of maternal origin by quantitative fluorescent polymerase chain reaction analysis following tissue culture failure for conventional cytogenetic analysis in a fetus with holoprosencephaly, ventricular septal defect, arthrogryposis of bilateral wrists and aplasia of the thumbs;Taiwanese Journal of Obstetrics and Gynecology;2021-05
3. Rapid Diagnosis of Trisomy 18 Using Uncultured Amniocytes in Late Second Trimester in a Pregnancy with Fetal Congenital Heart Defects, Arthrogryposis, Omphalocele, and Mega Cisterna Magna;Journal of Medical Ultrasound;2012-09
4. Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly;Taiwanese Journal of Obstetrics and Gynecology;2011-06
5. Prenatal Sonographic Features of Fetuses in Trisomy 13 Pregnancies (II);Taiwanese Journal of Obstetrics and Gynecology;2009-09
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