Trisomy 13/trisomy 18 mosaicism in an infant
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1996.tb02378.x/fullpdf
Reference9 articles.
1. Double autosomal trisomy and mosaicism for three cell lines in man;Garson;J Med Genet,1969
2. Double autosomal trisomy: case report (48, XX.+ 18 +21), and review of the literature;Grosse;J Ment Defic Res,1977
3. Origin of extra chromosome in Patau syndrome;Ishikiriyama;Hum Genet,1984
4. Trisomy 21 with 47, +18 lymphocyte cell line: double mitotic non-disjunction;Jenkins;J Med Genet,1978
5. Trisomy 21-trisomy 18 mosaicism in a boy with clinical Down syndrome;Marks;J Pediatr,1967
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1. Future Perspectives in Oxidative Stress in Trisomy 13 and 18 Evaluation;Journal of Clinical Medicine;2022-03-24
2. A child with complementary mosaic trisomy 8 and mosaic trisomy 21; clinical description of Warkany-Down syndrome and mechanism of origin;European Journal of Medical Genetics;2020-06
3. Prenatal diagnosis of a trisomy 7/trisomy 13 mosaicism;Molecular Cytogenetics;2012-01-27
4. Fetal trisomy 13 and 21 mosaicism diagnosed at amniocentesis: a case report;Prenatal Diagnosis;2009-06-29
5. A clinical report of a patient with two abnormal cell lines: 46,XX,del(21)(q22.1) and 47,XX,+3;American Journal of Medical Genetics Part A;2005-01-01
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