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Paper Details

Precise breakpoint detection in a patient with 9p- syndrome.
Cold Spring Harb Mol Case Stud
4
2020
9p- syndrome, Chr, Chr 13:50850492, Chr 9:1-190938, Chr 9:190938, Chromosome 13, Chromosome 9, FOXD4, PCDH9, RNASEH2B, ZIC2, autism, deletion and duplication regions, developmental delay, dysmorphic, genomic variants, patient
Author NameAffiliation
Robert S FultonMcDonnell Genome Institute, Washington University School of Medicine
Robert S FultonMcDonnell Genome Institute, Washington University School of Medicine
Francis Sessions ColeWashington University School of Medicine, and St. Louis Children's Hospital
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Release 1.2