An Unbalanced Translocation of Chromosome 16 Associated with Multiple Congenital Anomalies
Journal of the Korean Society of Neonatology
; : 212-216, 2005.
Article
在 Ko
| WPRIM
| ID: wpr-56293
Responsible library:
WPRO
ABSTRACT
We present a case of de novo reciprocal unbalanced translocation of chromosome 16, [46, XX, 8p+, der(8)t(8;16)(p23;q13)enh(16)], associated with clinical features, including anal atresia, vertebral anomaly, urogenital anomaly, single umbilical artery, ventricular septal defect and bilateral sensorineural hearing losses.
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