Search Results - Lorentz, Cindy P

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  1. 1
    Can incorporating molecular testing improve the accuracy of newborn screening for congenital adrenal hyperplasia?

    Can incorporating molecular testing improve the accuracy of newborn screening for congenital adrenal hyperplasia? by Sarafoglou, Kyriakie, Gaviglio, Amy, Wolf, Carrie, Lorentz, Cindy P, Lteif, Aida, Kyllo, Jennifer, Radloff, Gretchen, Detwiler, Zachary, Cuthbert, Carla D, Hodges, James S, Grosse, Scott D, Greene, Christopher N, Cordovado, Suzanne

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  2. 2
    Subtelomere deletions and translocations are frequently familial

    Subtelomere deletions and translocations are frequently familial by Adeyinka, Adewale, Adams, S. Annie, Lorentz, Cindy P., Van Dyke, Daniel L., Jalal, Syed M.

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    Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients

    Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients by Ensenauer, Regina E., Adeyinka, Adewale, Flynn, Heather C., Michels, Virginia V., Lindor, Noralane M., Dawson, D. Brian, Thorland, Erik C., Lorentz, Cindy Pham, Goldstein, Jennifer L., McDonald, Marie T., Smith, Wendy E., Simon-Fayard, Elba, Alexander, Alan A., Kulharya, Anita S., Ketterling, Rhett P., Clark, Robin D., Jalal, Syed M.

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