The phenotype of floating-harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP
SourceOrphanet Journal of Rare Diseases, 8, 1, (2013), pp. 63
Article / Letter to editor
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Orphanet Journal of Rare Diseases
SubjectIGMD 3: Genomic disorders and inherited multi-system disorders; NCMLS 6: Genetics and epigenetic pathways of disease IGMD 3: Genomic disorders and inherited multi-system disorders
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