1,395 results on '"Monaco, Anthony P."'
Search Results
52. Activation of ADP-ribosylation factor regulates biogenesis of the ATP7A-containing trans-Golgi network compartment and its Cu-induced trafficking
53. Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosis
54. Pooling for SARS-CoV2 Surveillance: Validation and Strategy for Implementation in K-12 Schools
55. Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits
56. Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT
57. Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia
58. A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States
59. Clinical features and molecular bases of neuroacanthocytosis
60. Autism: In search of susceptibility genes
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
63. Confirmatory evidence for linkage of relative hand skill to 2p12-q11. (Letters to the Editor)
64. A forkhead-domain gene is mutated in a severe speech and language disorder
65. Individual common variants exert weak effects on the risk for autism spectrum disorderspi
66. Investigation of Quantitative Measures Related to Reading Disability in a Large Sample of Sib-Pairs from the UK
67. Living Kidney Donation: Evolution and Technical Aspects of Donor Nephrectomy
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)
71. A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia)
72. Electronic identification and chromosomal assignment by radiation hybrid mapping of human expressed sequence tags corresponding to new potassium channel genes
73. Chorea-Acanthocytosis Genotype in the Original Critchley Kentucky Neuroacanthocytosis Kindred
74. Links between genetics and pathophysiology in the autism spectrum disorders
75. PCSK6 is associated with handedness in individuals with dyslexia
76. Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
77. An epigenetic, transgenerational model of increased mental health disorders in children, adolescents and young adults
78. Association of infantile convulsions with paroxysmal dyskinesias (ICCA syndrome): confirmation of linkage to human chromosome 16p12-q12 in a Chinese family
79. Molecular Genetic Investigations of Autism
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
83. Cell Biology of Membrane Trafficking in Human Disease
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
86. Mapping of Partially Overlapping de novo Deletions Across An Autism Susceptibility Region (AUTS5) in Two Unrelated Individuals Affected by Developmental Delays With Communication Impairment
87. Genetic influences on language impairment and phonological short-term memory
88. Generation of large insert yeast artificial chromosome libraries
89. Association of the KIAA0319 Dyslexia Susceptibility Gene With Reading Skills in the General Population
90. A Functional Genetic Link between Distinct Developmental Language Disorders
91. The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms
92. Choreoacanthocytosis in a Mexican Family
93. Multivariate Linkage Analysis of Specific Language Impairment (SLI)
94. Reducing the financial disincentives to living kidney donation: will compensation help the way it is supposed to?
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
96. Novel Delivery of Pancreatic Islet Cells to Treat Insulin-Dependent Diabetes Mellitus
97. Determination of the Mutation Spectrum of the EXT1/EXT2 Genes in British Caucasian Patients With Multiple Osteochondromas, and Exclusion of Six Candidate Genes in EXT Negative Cases
98. Use of an immune function assay to monitor immunosuppression for treatment of post-transplant lymphoproliferative disorder
99. The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
100. Construction of yeast artificial chromosome libraries by pulsed-field gel electrophoresis
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