Search Results - Starkovich, Molly

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  1. 1
    Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability

    Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability by Grau, Christina, Starkovich, Molly, Azamian, Mahshid S, Xia, Fan, Cheung, Sau Wai, Evans, Patricia, Henderson, Alex, Lalani, Seema R, Scott, Daryl A

    Published in PloS one
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  2. 2
    Chromosome 5q33 deletions associated with congenital heart defects

    Chromosome 5q33 deletions associated with congenital heart defects by Starkovich, Molly, Lalani, Seema R., Mercer, Catherine L., Scott, Daryl A.

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  3. 3
    The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia

    The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia by Jordan, Valerie K, Beck, Tyler F, Hernandez-Garcia, Andres, Kundert, Peter N, Kim, Bum-Jun, Jhangiani, Shalini N, Gambin, Tomasz, Starkovich, Molly, Punetha, Jaya, Paine, Ingrid S, Posey, Jennifer E, Li, Alexander H, Muzny, Donna, Hsu, Chih-Wei, Lashua, Amber J, Sun, Xin, Fernandes, Caraciolo J, Dickinson, Mary E, Lally, Kevin P, Gibbs, Richard A, Boerwinkle, Eric, Lupski, James R, Scott, Daryl A

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