Multiple congenital anomalies in a child born after prenatal diagnosis of trisomy 20mosaicism
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1986.tb01265.x/fullpdf
Reference16 articles.
1. Five cases of prenatally detected true mosaic trisomy 20.;Barbi;Hum. Genet.,1982
2. Trisomy 20 mosaicism in amniotic fluid cells.;Bösze;Pren. Diag.,1982
3. A familial F/G translocation (+ (20 p -; 22 q +)) observed in three generations.;Cohen;Clin. Genet.,1975
4. On the significance of true trisomy 20 mosaicism in amniotic fluid culture.;Djalali;Hum. Genet.,1985
5. Further examples of trisomy-20 mosaicism in amniotic cell cultures.;Grewal;Pren. Diag.,1985
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1. Additional Evidence for Neuropsychiatric Manifestations in Mosaic Trisomy 20: A Case Report and Brief Review;Children;2021-11-10
2. Mosaic trisomy 20 and mitigation in capital crimes sentencing: A review and case report;Behavioral Sciences & the Law;2019-08-07
3. Trisomy 5 mosaicism in amniotic fluid with normal outcome;Clinical Genetics;2008-06-28
4. Non-mosaic trisomy 20 in amniotic fluid cultures with minor anomalies in the fetus;Clinical Genetics;2008-06-28
5. Expanding the phenotype of mosaic trisomy 20;American Journal of Medical Genetics Part A;2008
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