Refinement of causative genes in monosomy 1p36 through clinical and molecular cytogenetic characterization of small interstitial deletions by Rosenfeld, Jill A., Crolla, John A., Tomkins, Susan, Bader, Patricia, Morrow, Bernice, Gorski, Jerome, Troxell, Robin, Forster-Gibson, Cynthia, Cilliers, Deirdre, Hislop, R. Gordon, Lamb, Allen, Torchia, Beth, Ballif, Blake C., Shaffer, Lisa G.

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Disruption of Neurexin 1 Associated with Autism Spectrum Disorder by Kim, Hyung-Goo, Kishikawa, Shotaro, Higgins, Anne W., Seong, Ihn-Sik, Donovan, Diana J., Shen, Yiping, Lally, Eric, Weiss, Lauren A., Najm, Juliane, Kutsche, Kerstin, Descartes, Maria, Holt, Lynn, Braddock, Stephen, Troxell, Robin, Kaplan, Lee, Volkmar, Fred, Klin, Ami, Tsatsanis, Katherine, Harris, David J., Noens, Ilse, Pauls, David L., Daly, Mark J., MacDonald, Marcy E., Morton, Cynthia C., Quade, Bradley J., Gusella, James F.

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Refinement of Causative Genes in Monosom 1p36 Through Clinical and Molecular Cytogenetic Characterization of Small Interstitial Deletions by ROSENFELD, Jill A, CROLLA, John A, LAMB, Allen, TORCHIA, Beth, BALLIF, Blake C, SHAFFER, Lisa G, TOMKINS, Susan, BADER, Patricia, MORROW, Bernice, GORSKI, Jerome, TROXELL, Robin, FORSTER-GIBSON, Cynthia, CILLIERS, Deirdre, HISLOP, R. Gordon

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