A severely retarded child with multiple malformations was found to present a mosaic karyotype 46,XX, - 13,+t(13;13)(p11;q11)/46,XX,del(13)(p11), which probably originated as the result of a de novo 13/13 translocation in a parental gamete, followed by postzygotic fission of the translocation chromos
Trisomy 18q: 46, XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46, XY,-13,+der(13)/t(13;18)(q32;q11)
โ Scribed by D. S. Krishna Murthy; Z. M. Patel; L. M. Ambani
- Book ID
- 119839033
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 442 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0009-9163
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