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	1.	Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family. [electronic resource] by Amador, Claudia Mathews, Anne M Del Carmen Montoya, Maria Laughridge, Mary E Everman, David B Holden, Kenton R Producer: 20081017 In: Journal of child neurology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation. [electronic resource] 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 Producer: 20061128 In: American journal of medical genetics. Part A vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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