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Orphanet Journal of Rare Diseases
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April 30, 2013
The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP
Sarah M Nikkel, Andrew Dauber, Sonja de Munnik, et al.
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of 3
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Showing results (21-30 of 21) with videos related to
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Orphanet Journal of Rare Diseases
|
April 30, 2013
The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP
Sarah M Nikkel, Andrew Dauber, Sonja de Munnik, et al.
Page
of 3