Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole‐genome sequencing
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V. Jobanputra | C. Morton | M. Talkowski | V. Aggarwal | Z. Ordulu | V. Pillalamarri | C. Hanscom | S. Pereira | B. Levy | M. Macera | D. Warburton | A. Sobrino | A. Mills | C. Esteves | Zehra Ordulu | Carrie Hanscom