Search Results - Laughridge, Mary E.

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  1. 1
    Expanding the Neurologic Phenotype of Oculodentodigital Dysplasia in a 4-Generation Hispanic Family

    Expanding the Neurologic Phenotype of Oculodentodigital Dysplasia in a 4-Generation Hispanic Family by 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

    Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation by 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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