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PRDM13 exome sequencing set

Exome sequencing study on 4 individuals from a pedigree with CHH and cerebellar hypoplasia.

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Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.

Study ID Study Title Study Type
EGAS00001005878 Other

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID File Type Size Located in
EGAF00005740419 fq.gz 4.2 GB
EGAF00005740420 fq.gz 5.1 GB
EGAF00005740421 fq.gz 5.2 GB
EGAF00005740422 fq.gz 4.5 GB
EGAF00005740423 fq.gz 5.8 GB
EGAF00005740424 fq.gz 5.1 GB
EGAF00005740425 fq.gz 4.6 GB
EGAF00005740426 fq.gz 4.8 GB
8 Files (39.3 GB)