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Items: 3

1.

Clinically Relevant Copy Number Variations Detected in Cerebral Palsy

(Submitter supplied) Cerebral palsy (CP) represents a group of non-progressive clinically heterogeneous disorders that are characterized by motor impairment and early age-of-onset, frequently accompanied by co-morbidities. The cause of CP has historically been attributed to environmental stressors resulting in brain damage. While genetic risk factors are also implicated, guidelines for diagnostic assessment of CP do not recommend for routine genetic testing. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platform:
GPL20641
429 Samples
Download data: TXT
Series
Accession:
GSE70374
ID:
200070374

PubMed Full text in PMC Similar studies

2.

Illumina HumanOmni2.5M-8v1-1_B [data table]

(Submitter supplied) Illumina HumanOmni25M-8v1-1_B Protocol: see Illumina web site
Organism:
Homo sapiens
9 Series
612 Samples
Download data: BPM, CSV
Platform
Accession:
GPL20641
ID:
100020641

3.

4-24M

Organism:
Homo sapiens
Source name:
Saliva
Platform:
GPL20641
Series:
GSE70374
Download data
Sample
Accession:
GSM1726976
ID:
301726976

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db=gds|term=GSM1726976[Accession]|query=1|qty=2|blobid=MCID_6749652f4e6f392e263d4900|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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