Initial approaches to prenatal diagnosis from fetal karyotyping involved application of standard cytogenetic techniques. However, when fetal samples, such as chorionic villus cells or amniocytes are used, small chromosome rearrangements cannot be easily identified because they lack a distinct bandin
โฆ LIBER โฆ
Detection of chromosome 18 rearrangement in synovial sarcoma by fluorescence in situ hybridization
โ Scribed by Harry T. Poteat; Joseph M. Corson; Jonathan A. Fletcher
- Book ID
- 113253573
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 441 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0165-4608
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