Pediatric Laryngeal Diadochokinetic Rates: Establishing a Normative Database by Maturo, Steve, Hill, Courtney, Bunting, Glenn, Ballif, Cathy, Maurer, Rie, Hartnick, Christopher

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Pediatric Laryngeal Diadochokinetic Rates by Maturo, Steve, Hill, Courtney, Bunting, Glenn, Ballif, Cathy, Maurer, Rie, Hartnick, Christopher

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Investigation of NRXN1 deletions: Clinical and molecular characterization by Dabell, Mindy Preston, Rosenfeld, Jill A., Bader, Patricia, Escobar, Luis F., El-Khechen, Dima, Vallee, Stephanie E., Dinulos, Mary Beth Palko, Curry, Cynthia, Fisher, Jamie, Tervo, Raymond, Hannibal, Mark C., Siefkas, Kiana, Wyatt, Philip R., Hughes, Lauren, Smith, Rosemarie, Ellingwood, Sara, Lacassie, Yves, Stroud, Tracy, Farrell, Sandra A., Sanchez-Lara, Pedro A., Randolph, Linda M., Niyazov, Dmitriy, Stevens, Cathy A., Schoonveld, Cheri, Skidmore, David, MacKay, Sara, Miles, Judith H., Moodley, Manikum, Huillet, Adam, Neill, Nicholas J., Ellison, Jay W., Ballif, Blake C., Shaffer, Lisa G.

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Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes by Rosenfeld, Jill A, Traylor, Ryan N, Schaefer, G Bradley, McPherson, Elizabeth W, Ballif, Blake C, Klopocki, Eva, Mundlos, Stefan, Shaffer, Lisa G, Aylsworth, Arthur S

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Genotype–phenotype correlation in interstitial 6q deletions: a report of 12 new cases by Rosenfeld, Jill A., Amrom, Dina, Andermann, Eva, Andermann, Frederick, Veilleux, Martin, Curry, Cynthia, Fisher, Jamie, Deputy, Stephen, Aylsworth, Arthur S., Powell, Cynthia M., Manickam, Kandamurugu, Heese, Bryce, Maisenbacher, Melissa, Stevens, Cathy, Ellison, Jay W., Upton, Sheila, Moeschler, John, Torres-Martinez, Wilfredo, Stevens, Abby, Marion, Robert, Pereira, Elaine Maria, Babcock, Melanie, Morrow, Bernice, Sahoo, Trilochan, Lamb, Allen N., Ballif, Blake C., Paciorkowski, Alex R., Shaffer, Lisa G.

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