Amniocentesis on a 32-year-old woman at risk for trisomy 21 by maternal serum triple screen showed a 46,Y,inv(X) (p22.1q24) karyotype in all cells analyzed. A blood sample was obtained from the mother for cytogenetic evaluation. Since she had the same inversion, DNA replication studies were performe
Prenatal detection of an inverted X chromosome in a male fetus
✍ Scribed by Rosário Pinto Leite; Maximina Pinto
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 35 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0197-3851
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