A supernumerary extra chromosome of maternal origin, precisely described from QM- and C-banding patterns, was studied in a mentally defective boy with a severe convulsive disorder. This case is considered to represent a specific phenotype of trisomy 15q1. The suggestion that in cases of partial tris
Partial trisomy 12g15…q22
✍ Scribed by Z. Yilmaz; M. Erman-Akar; S. Ceylaner; G. Ceylaner; S. Nabaei; O. Gökmen
- Book ID
- 117124981
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 159 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0020-7292
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Partial trisomy 15 was observed in a newborn with malformations of the head and extremities. A t(5;15) translocation was found in the mother and maternal grandfather.
## Abstract Interchromosomal insertional translocations are rare chromosome rearrangements with an incidence of about 1:80,000 live births. We report on the clinical and cytogenetic findings of a newborn baby with partial trisomy 10q22–10q24 due to a maternal insertional translocation 15;10. Partia
T w o sibs, carriers of unbalanced products of the translocation t(15;21)(915;q22.l)pat, are described. The sister had Prader-Willi syndrome due to deletion 15 (pter > q15) and partial trisomy 21 (pter > q22.1); her brother had partial trisomy 15 (pter > q15) and partial monosomy 21 (pter > q22.1).