Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families von Doll, Julia, Vona, Barbara, Schnapp, Linda, Rüschendorf, Franz, Khan, Imran, Khan, Saadullah, Muhammad, Noor, Alam Khan, Sher, Nawaz, Hamed, Khan, Ajmal, Ahmad, Naseer, Kolb, Susanne M., Kühlewein, Laura, Labonne, Jonathan D. J., Layman, Lawrence C., Hofrichter, Michaela A. H., Röder, Tabea, Dittrich, Marcus, Müller, Tobias, Graves, Tyler D., Kong, Il-Keun, Nanda, Indrajit, Kim, Hyung-Goo, Haaf, Thomas

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The long and short of the S-locus in Turnera (Passifloraceae) von Shore, Joel S., Hamam, Hasan J., Chafe, Paul D. J., Labonne, Jonathan D. J., Henning, Paige M., McCubbin, Andrew G.

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An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability von Labonne, Jonathan D. J., Lee, Kang-Han, Iwase, Shigeki, Kong, Il-Keun, Diamond, Michael P., Layman, Lawrence C., Kim, Cheol-Hee, Kim, Hyung-Goo

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A microdeletion at Xq22.2 implicates a glycine receptor GLRA4 involved in intellectual disability, behavioral problems and craniofacial anomalies von Labonne, Jonathan D J, Graves, Tyler D, Shen, Yiping, Jones, Julie R, Kong, Il-Keun, Layman, Lawrence C, Kim, Hyung-Goo

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Concomitant partial exon skipping by a unique missense mutation of RPS6KA3 causes Coffin–Lowry syndrome von Labonne, Jonathan D.J., Chung, Min Ji, Jones, Julie R., Anand, Priya, Wenzel, Wolfgang, Iacoboni, Daniela, Layman, Lawrence C., Kim, Hyung-Goo

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A microdeletion encompassing PHF21A in an individual with global developmental delay and craniofacial anomalies von Labonne, Jonathan D. J., Vogt, Julie, Reali, Lisa, Kong, Il-Keun, Layman, Lawrence C., Kim, Hyung-Goo

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Comparative Genomic Mapping Implicates LRRK2 for Intellectual Disability and Autism at 12q12, and HDHD1, as Well as PNPLA4, for X-Linked Intellectual Disability at Xp22.31 von Labonne, Jonathan D J, Driessen, Terri M, Harris, Marvin E, Kong, Il-Keun, Brakta, Soumia, Theisen, John, Sangare, Modibo, Layman, Lawrence C, Kim, Cheol-Hee, Lim, Janghoo, Kim, Hyung-Goo

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Positional cloning of the s haplotype determining the floral and incompatibility phenotype of the long-styled morph of distylous Turnera subulata von Labonne, Jonathan D. J, Shore, Joel S

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Steric Clash in the SET Domain of Histone Methyltransferase NSD1 as a Cause of Sotos Syndrome and Its Genetic Heterogeneity in a Brazilian Cohort von Ha, Kyungsoo, Anand, Priya, Lee, Jennifer A, Jones, Julie R, Kim, Chong Ae, Bertola, Debora Romeo, Labonne, Jonathan D J, Layman, Lawrence C, Wenzel, Wolfgang, Kim, Hyung-Goo

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Comparative deletion mapping at 1p31.3-p32.2 implies NFIA responsible for intellectual disability coupled with macrocephaly and the presence of several other genes for syndromic in... von Labonne, Jonathan D J, Shen, Yiping, Kong, Il-Keun, Diamond, Michael P, Layman, Lawrence C, Kim, Hyung-Goo

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Changes in nucleosome position at transcriptional start sites of specific genes in Zea mays mediator of paramutation1 mutants von Labonne, Jonathan D J, Dorweiler, Jane E, McGinnis, Karen M

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