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Partial trisomy 6p and partial monosomy 9p from a de novo translocation 46, XY, -9, + DER(9)T(6:9)(p211:p24)

✍ Scribed by Melanie S. Eden; James W. Thelin; Karen Michalski; Joyce A. Mitchell

Book ID
115089306
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
629 KB
Volume
28
Category
Article
ISSN
0009-9163

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Trisomy 9p resulting from de novo 9/15 t
Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome
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Trisomy 9p with de novo 9/15 translocation and 9p isochromosome was observed in a mentally defective boy with typical clinical features for this syndrome. This chromosomal aberration is probably caused by the pericentric inversion of chromosome 9 of the patient's father.

Case of partial trisomy 9p and partial t
Case of partial trisomy 9p and partial trisomy 14q resulting from a maternal translocation: Overlapping manifestations of characteristic phenotypes
✍ Angle, Brad; Yen, Frank; Cole, Cameron W. πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 31 KB πŸ‘ 2 views

We report on a female infant with partial trisomy 9p (pter→p13) and partial trisomy 14q (pter→q22) resulting from a 3:1 segregation of a maternal reciprocal translocation (9;14)(p13;q22). Both trisomy 9p and partial trisomy 14q have been described as recognized phenotypes with characteristic pattern