Prenatal diagnosis of 46, XX/47, XXY mosaicism: A case report
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference9 articles.
1. True hermaphroditism with bilateral ovotestis: a case report
2. European collaborative study on prenatal diagnosis: Mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell cultures
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4. (1986). Prenatal diagnosis of chromosome abnormalities. In: (Ed.). Genetic Disorders and the Fetus, New York: Plenum Press, 115–183.
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1. Klinefelter Syndrome Mosaicism 46,XX/47,XXY: A New Case and Literature Review;Journal of Pediatric Genetics;2020-06-17
2. Rare XXY/XX mosaicism in a phenotypic male presenting as cystic hygroma in the first trimester;Clinical Dysmorphology;2017-04
3. Prenatal Diagnosis of Sex Chromosome Abnormalities;Genetic Disorders and the Fetus;2015-11-23
4. Prenatal Diagnosis of Sex Chromosome Abnormalities;Genetic Disorders and the Fetus;2010-09-24
5. Rare XXY/XX mosaicism in a phenotypic male with Klinefelter syndrome: case report;European Journal of Medical Genetics;2006-07
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