DRD2 and PPP1R1B (DARPP-32) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in male-only affected sib-pair fa... von Hettinger, Joe A, Liu, Xudong, Hudson, Melissa L, Lee, Alana, Cohen, Ira L, Michaelis, Ron C, Schwartz, Charles E, Lewis, Suzanne M E, Holden, Jeanette J A

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A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families von Hettinger, Joe A., Liu, Xudong, Schwartz, Charles E., Michaelis, Ron C., Holden, Jeanette J.A.

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De novo 5q35.5 duplication with clinical presentation of Sotos syndrome von Kasnauskiene, Jurate, Cimbalistiene, Loreta, Ciuladaite, Zivile, Preiksaitiene, Egle, Kučinskienė, Zita Aušrelė, Hettinger, Joe A., Sismani, Carolina, Patsalis, Philippos C., Kučinskas, Vaidutis

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The G22A Polymorphism of the ADA Gene and Susceptibility to Autism Spectrum Disorders von Hettinger, Joe A., Liu, Xudong, Holden, Jeanette Jeltje Anne

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Unbalanced Translocations Involving Chromosome Region 10q25.3q26.3 in Patients with Intellectual Disability and Complex Phenotypes von Hryshchenko, Nataliya V., Bychkova, Ganna M., Tavokina, Lyubov V., Brovko, Anton O., Graziano, Claudio, Soloviov, Oleksandr O., Hettinger, Joe A., Patsalis, Philippos C., Lurie, Iosif W., Livshits, Ludmila A.

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A Novel Arginine Vasopressin-Neurophysin II Mutation Causes Autosomal Dominant Neurohypophyseal Diabetes insipidus and Morphologic Pituitary Changes von Skordis, Nicos, Patsalis, Philippos C., Hettinger, Joe A., Kontou, Maria, Herakleous, Eleni, Krishnamani, M.R.S., Phillips III, J.A.

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De novo 5q35.5 duplication with clinical presentation of Sotos syndrome von Kasnauskiene, Jurate, Cimbalistiene, Loreta, Ciuladaite, Zivile, Preiksaitiene, Egle, Kučinskienė, Zita Aušrelė, Hettinger, Joe A., Sismani, Carolina, Patsalis, Philippos C., Kučinskas, Vaidutis

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Frequencies of "grey-zone" and premutation-size FMR1 CGG-repeat alleles in patients with developmental disability in Cyprus and Canada von Patsalis, Philippos C., Sismani, Carolina, Hettinger, Joe A., Holden, Jeanette J.A., Lawson, J. Stuart, Chalifoux, Maryse, Wing, Maggie, Walker, Melissa, Leggo, Jayne

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Frequencies of ?grey-zone? and premutation-sizeFMR1 CGG-repeat alleles in patients with developmental disability in Cyprus and Canada von Patsalis, Philippos C., Sismani, Carolina, Hettinger, Joe A., Holden, Jeanette J.A., Lawson, J. Stuart, Chalifoux, Maryse, Wing, Maggie, Walker, Melissa, Leggo, Jayne

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