A 10 1/2-month-old boy was found to have an unbalanced karyotype, 45,XY,der(8)t(8;15) (p23.3;q13). One of 83 analyzed cells also contained an unidentified small marker. Fluorescence in situ hybridization (FISH) using cosmid probes for SNRPN, D15S10, and GABRB3 for the Prader-Willi syndrome (PWS)/Ang
A survey of inherited thrombotic syndromes in italy
β Scribed by Armando Tripodi; Pier Mannuccio Mannucci
- Publisher
- Springer
- Year
- 1989
- Tongue
- English
- Weight
- 454 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0940-5437
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