Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing

Authors :: Macera, M.J.
Sobrino, A.
Levy, B.
Jobanputra, V.
Aggarwal, V.
Mills, A.
Esteves, C.
Hanscom, C.
Pereira, S.
Pillalamarri, V.
Ordulu, Z.
Morton, C.
Talkowski, M.
Warburton, D.
Publication Year :: 2015

Subjects :: Adult
Genome
Chromosome Disorders
Sequence Analysis, DNA
Article
Translocation, Genetic
Pregnancy
Karyotyping
Prenatal Diagnosis
Humans
Abnormalities, Multiple
Female
In Situ Hybridization, Fluorescence
Oligonucleotide Array Sequence Analysis

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