Expanding the Neurologic Phenotype of Oculodentodigital Dysplasia in a 4-Generation Hispanic Family von Amador, Claudia, Mathews, Anne M., del Carmen Montoya, Maria, Laughridge, Mary E., Everman, David B., Holden, Kenton R.

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Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation von Everman, David B., Morgan, Chad T., Lyle, Robert, Laughridge, Mary E., Bamshad, Michael J., Clarkson, Katie B., Colby, Randall, Gurrieri, Fiorella, Innes, A. Micheil, Roberson, Jacquelyn, Schrander-Stumpel, Connie, van Bokhoven, Hans, Antonarakis, Stylianos E., Schwartz, Charles E.

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