## 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 10q22β10q24 due to a maternal insertional translocation 15;10. Partia
Partial monosomy 10q and partial trisomy 9q with anal atresia due to maternal translocation: t(9;10)(q32;q26)
β Scribed by Toshinori Tsukuda; Ikuo Nagata; Hiroshi Sawada; Jun Murakami; Keiichi Hanaki; Hirofumi Urashima; Tomoharu Kaneda; Norio Shimizu; Nobuaki Kaibara; Nagao Kodama; Takehiko Ohzeki; Kazuo Shiraki
- Book ID
- 115091837
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 282 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0009-9163
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π SIMILAR VOLUMES
A new case of partial trisomy for the long arm of chromosome 1 was observed in a newborn female, who died at age 26 days. The father was a proven carrier of a balanced translocation involving chromosomes 1 and 10.
A family is reported in which the propositus has an extra G-like chromosome with an unusual G-banding pattern. Cytogenetic family studies showed that the mother is a carrier of a balanced reciprocal translocation t(13;22), which does not affect the size and morphology of the chromosomes involved. Th