Another case of prenatally diagnosed 48,XYY,+21
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference24 articles.
1. THE CHROMOSOMES IN A PATIENT SHOWING BOTH MONGOLISM AND THE KLINEFELTER SYNDROME
2. Prenatal diagnosis of 48,XYY, + 21 ascertained through ultrasound anomalies
Cited by 4 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. Familial small supernumerary marker chromosome (sSMC) (14)(:P11–q11:)In a child with translocation down syndrome;The Indian Journal of Pediatrics;2009-12
2. Epidemiology of double aneuploidies involving chromosome 21 and the sex chromosomes;American Journal of Medical Genetics Part A;2005
3. First patient with trisomy 21 accompanied by an additional der(4)(:p11 ? q11:) plus partial uniparental disomy 4p15-16;American Journal of Medical Genetics;2002-12-10
4. MISINTERPRETATION OF TRISOMY 18 AS A PSEUDOMOSAICISM AT THIRD-TRIMESTER AMNIOCENTESIS OF A CHILD WITH A MOSAIC 46,XY/47,XY,+3/48,XXY,+18 KARYOTYPE;Prenatal Diagnosis;1997-04
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