Next-generation Sequencing and Karyotype Analysis for the Diagnosis of Robertsonian Translocation Type Trisomy 13: A Case Report

• Egile Nagusiak: Jing SHA (Egilea), Fumin LIU (Egilea), Bei ZHANG (Egilea), Yang HUANG (Egilea), Qinglin ZHANG (Egilea), Gao JUAN (Egilea), Jingfang ZHAI (Egilea)
• Formatua: Liburua
• Argitaratua: Tehran University of Medical Sciences, 2017-05-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

Trisomy 13 (Patau syndrome) is the third most common autosomal trisomy with a prevalence between 1 in 10,000 - 20,000 live births. Robertsonian translocations represent the largest number of chromosomal aberrations in human population with an incidence of 1.23 in 1000 live birth and translocation 13...