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52. Activation of ADP-ribosylation factor regulates biogenesis of the ATP7A-containing trans-Golgi network compartment and its Cu-induced trafficking

55. Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

57. Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

61. A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11

62. Use of multivariate linkage analysis for dissection of a complex cognitive trait

65. Individual common variants exert weak effects on the risk for autism spectrum disorderspi

68. Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. (Report)

69. A genomewide scan for loci involved in attention-deficit/ hyperactivity disorder

70. A genomewide linkage screen for relative hand skill in sibling pairs. (Report)

76. Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

80. Identification of FOXP1 Deletions in Three Unrelated Patients with Mental Retardation and Significant Speech and Language Deficits

81. A genome-wide scan for common alleles affecting risk for autism

82. Functional impact of global rare copy number variation in autism spectrum disorders

84. A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia

85. A genome-wide linkage and association scan reveals novel loci for autism

92. Choreoacanthocytosis in a Mexican Family

95. Refined genetic mapping of the Darier locus to a <1-cM region of chromosome 12q24.1, and construction of a complete, high-resolution P1 artificial chromosome/bacterial artificial chromosome contig of the critical region

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