Double trisomy (48,XXX, +18)
- PMID: 7802021
- DOI: 10.1002/ajmg.1320520227
Double trisomy (48,XXX, +18)
Comment on
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An infant with double trisomy (48,XXX, + 18).Am J Med Genet. 1994 Jan 15;49(2):207-10. doi: 10.1002/ajmg.1320490210. Am J Med Genet. 1994. PMID: 8116670 Review.
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An infant with double trisomy (48,XXX, + 18).Am J Med Genet. 1994 Jan 15;49(2):207-10. doi: 10.1002/ajmg.1320490210. Am J Med Genet. 1994. PMID: 8116670 Review.
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Trisomy 18 with unilateral atypical ectrodactyly.Am J Med Genet. 1994 Jan 1;49(1):125-7. doi: 10.1002/ajmg.1320490125. Am J Med Genet. 1994. PMID: 8172239 No abstract available.
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Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.Ann Genet. 1989;32(3):177-9. Ann Genet. 1989. PMID: 2486064
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A case of 48, XXX, +18 double trisomy.Acta Paediatr Jpn. 1987 Feb;29(1):178-81. doi: 10.1111/j.1442-200x.1987.tb00027.x. Acta Paediatr Jpn. 1987. PMID: 3144845 Review. No abstract available.
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Clinical and postmortem findings of two cases with karyotype: 48, XXX, +18.Acta Paediatr Jpn. 1987 Feb;29(1):173-7. doi: 10.1111/j.1442-200x.1987.tb00026.x. Acta Paediatr Jpn. 1987. PMID: 3144844 No abstract available.
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Double trisomy 48,XXX,+18 with multiple dysmorphic features.World J Pediatr. 2015 Feb;11(1):83-8. doi: 10.1007/s12519-015-0005-7. Epub 2015 Jan 28. World J Pediatr. 2015. PMID: 25822702
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Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21.J Med Genet. 1995 Aug;32(8):650-3. doi: 10.1136/jmg.32.8.650. J Med Genet. 1995. PMID: 7473661 Free PMC article.
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