The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP
2013 · Orphanet Journal of Rare Diseases · 83 citations
https://doi.org/10.1186/1750-1172-8-63
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Meghan Connolly is an academic researcher. The author has contributed to research in topics: Genetic and rare skin diseases. & Congenital limb and hand anomalies & Cystic Fibrosis Research Advances. The author has an h-index of 2, co-authored 3 publications.
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