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Accession: PRJNA286132 ID: 286132

Homo sapiens (human)

Genome-wide association study on craniofacial microsomia

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Craniofacial microsomia encapsulates congenital anomalies of the external and middle ear, maxilla, mandible, facial and trigeminal nerves, and surrounding soft tissues on the affected side. More...
AccessionPRJNA286132; GEO: GSE69664
Data TypeVariation
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsZhang YB et al., "Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.", Nat Commun, 2016 Feb 8;7:10605
SubmissionRegistration date: 8-Jun-2015
Beijing Institute of Genomics
RelevanceMedical
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PMC1
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Data volume, Supplementary Mbytes20310

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