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Uniparental disomy and the phenotype of mosaic trisomy 20: a new case and review of the literature

โœ Scribed by Z. Powis; R. P. Erickson


Publisher
Springer-Verlag
Year
2009
Tongue
English
Weight
94 KB
Volume
50
Category
Article
ISSN
1234-1983

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Mosaic trisomy 22: A case presentation a
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I have read with great interest the paper by Crowe et al. [1997]. It is an excellent clinical and cytogenetic review of trisomy 22 in its various manifestations. I only wish to point out that the first proven case (by G-banding) of trisomy 22 appeared in 1973, in a paper in which we demonstrated the

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## Abstract Trisomy 13, or Patau syndrome is a rare chromosomal disorder characterized by a triad of cleft lip and palate, postaxial polydactyly and microcephaly. Complete, partial, or mosaic forms of the disorder can occur. Mosaic trisomy 13 is very rare, it occurs in only 5% of all patients with