A familial F/G translocation [t(20p-; 22q+)] observed in three generations
β Scribed by Maimon M. Cohen; Ronald G. Davidson; Judith A. Brown
- Book ID
- 119838199
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 557 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0009-9163
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A case of an inherited type of D/G translocation D1-trisomy syndrome was described. A female proposita who had the clinical signs of D1-trisomy syndrome was found to have a chromosome complement of 46,XX,--G,+t(DqGq). examination of Q- and G-stained karyotypes revealed that the chromosomes involved
A case of partial trisomy 9 is described in a mentally retarded and dysmorphic child, confirming that this chromosome unbalance results in a characteristic clinical entity. This trisomy arose through aberrant segregation of translocation chromosome during meiosis in the patient's mother, who is a ba
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