Roberto Mendoza-Londono has
Featured publications View all
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Article: Mutations in B3GALT6, which Encodes a Glycosaminoglycan Linker Region Enzyme, Cause a Spectrum of Skeletal and Connective Tissue Disorders.
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Article: Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder.
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Article: Osteopathia striata with cranial sclerosis and developmental delay in a male with a mosaic deletion in chromosome region Xq11.2.
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