Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome.
until further notice
SourceClinical Genetics, 77, 4, (2010), pp. 404-407
1 april 2010
Article / Letter to editor
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SubjectDCN 2: Functional Neurogenomics; IGMD 3: Genomic disorders and inherited multi-system disorders; NCMLS 6: Genetics and epigenetic pathways of disease
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